Recalls & alerts

1278 alerts recorded, refreshed every six hours. Filter by source or category.

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openFDA · August 19, 2026Moderate risk
W L Gore & Associates, Inc. : GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1006. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…
The recall affects GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1006, distributed in Georgia and Rhode Island. The device may be mislabeled as a different size and type, posing a risk of incorrect placement for patients needing bile duct treatment. Consumers and healthcare providers should stop using the device, verify the label, and contact W L Gore & Associates for return instructions.
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB
Cardinal Health Presource Kits, specifically the NEWNAN SMR PACK with catalog number SEN21SPPMB, are affected. The kits contain MEDICOM Ritmed Neurological Sponges with unexpected variability in endotoxin levels, exposing patients to potential harm. Consumers should stop using these kits and follow the firm's recall instructions for return or disposal.
devices
openFDA · August 19, 2026Moderate risk
Straumann USA LLC : Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form
Straumann USA LLC is recalling its Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314). The implant may actually be 12mm long instead of the labeled 14mm, posing a risk to patients receiving this dental device. Consumers should contact their dentist or Straumann to determine if their implant is affected and what to do next.
devices
openFDA · August 19, 2026Moderate risk
Covidien, LP : V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12…
Covidien is recalling its V-Loc 90 Absorbable Wound Closure Device sutures. The sterile barrier packaging may have a tear or perforation, risking contamination and infection for patients, including vision loss in eye surgery. Consumers should stop using affected lots and contact Covidien for return or replacement.
devices
openFDA · August 19, 2026Moderate risk
Erbe USA Inc : ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
The recalled product is the Erbe USA Inc ERBECRYO 2 Cryosurgical Unit, model/catalog number 10402-000. A strong pull on the high-pressure transfer hose can cause a pneumatic short circuit, leading to CO2 leaking into the return path and excessive pressure that may rupture the cryoprobe, exposing patients and operators to injury. Consumers must comply with the voluntary recall initiated by the firm.
devices
openFDA · August 19, 2026Moderate risk
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. : Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 and R3.1;…
Philips Azurion interventional fluoroscopic x-ray systems, model numbers 722229 through 722236 with software versions R3.0 and R3.1, are affected. Two software issues can degrade image quality or cause loss of geometry movements, leading to delayed therapy, procedural complications, or inappropriate treatment for patients. Consumers should contact their healthcare provider or Philips for instructions on the voluntary recall.
devices
openFDA · August 19, 2026Moderate risk
Remel Europe Ltd. : Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics
Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, product number R30166901, is affected. Certain lots do not perform to the intended criteria, which could cause false test results for patients. Users should check their lot numbers and follow the firm's recall instructions.
devices
openFDA · August 19, 2026Moderate risk
Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN
Medline Industries is recalling Medline Micro-Kill Bleach Germicidal Bleach Wipes, 7 by 8 inches, 150 count, product number MSC351400AN. The wipes may lose bleach
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI…
Cardinal Health Presource Kits, including specific catalog numbers for neuro, nasal, and ENT procedures, are affected. The kits contain Medicom Ritmed Neurological Sponges with unexpected endotoxin levels, exposing patients to potential infection or adverse reactions. Consumers should stop using the affected kits, verify catalog numbers, and contact Cardinal Health for instructions.
devices
openFDA · August 19, 2026Moderate risk
Ventana Medical Systems, Inc. : navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code:…
Ventana Medical Systems (Roche) is recalling navify Digital Pathology software v2.5, both on-prem and Cloud versions. The software can show image/metadata discrepancies in the Viewer window, affecting pathologists and healthcare providers using the system. Consumers should stop using the affected software and contact the firm for correction or replacement.
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD , Catalog Number: 21-4720C; 3) KIT,BOSC…
Cardinal Health is recalling its Presource procedure kits, including fat graft, nasal pack, spine, neuro, and craniotomy packs. The kits contain Medicom Ritmed Neurological Sponges with unexpected endotoxin variability, exposing patients to risk during procedures. Consumers should stop using affected kits, check catalog numbers, and contact Cardinal Health for return instructions.
devices
openFDA · August 19, 2026Moderate risk
Covidien, LP : Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX
Covidien, LP is recalling its Surgipro II S8698GX sutures (SURGIPRO II BL 5/0 18 P-13). The sterile packaging may have a tear or perforation, exposing patients to contaminated sutures that can cause infection, vision loss in eye surgery, or longer operations. Consumers should stop using the affected product and contact Covidien for return and replacement instructions.
devices
openFDA · August 19, 2026Moderate risk
Galt Medical Corporation : Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/…
Boston Scientific is recalling its Enhance Transcarotid/Peripheral Access Kit, model REF SR-4F21G7D-MP. The black depth markings on the sheath can detach, posing a risk to patients during procedures. Patients or users should contact their healthcare provider to arrange return or replacement.
devices
openFDA · August 19, 2026High risk
Baxter Healthcare Corporation : Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Baxter Healthcare Corporation is recalling its Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507, and Solution Administration Sets. The devices can produce air bubbles in the drip chamber and tubing when a pressure cuff is used or the tubing is flushed fully open, posing a risk to patients. Consumers should stop using the affected products and contact Baxter Healthcare for further instructions.
devices
openFDA · August 19, 2026High risk
Spectra Medical Devices, Llc : Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride…
Spectra Medical Devices' Elevaris brand Sodium Chloride Injection 0.9% USP 10mL Ampule is recalled. The product may have compromised sterility, exposing patients using it for IV tubing and indwelling intravascular access devices to microorganisms, endotoxins, or foreign matter, which can cause infections or organ failure. Consumers should stop using the recalled ampules and follow the firm's recall instructions.
devices
openFDA · August 19, 2026Moderate risk
Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
Medline Industries is recalling its Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, product number MSC351410AN. The wipes may lose bleach strength before the 12-month shelf life ends, reducing disinfection and allowing harmful germs to survive, which poses a risk to users. Consumers should stop using the wipes and contact Medline for a refund or replacement.
devices
openFDA · August 19, 2026Moderate risk
Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
Medline Industries is recalling Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12 by 12 inches, 110 count, product number MSC351450AN. The wipes may lose bleach strength before their 12-month shelf life ends, reducing disinfection and allowing harmful germs to survive, which poses a risk to users. Consumers should stop using the affected wipes and contact Medline for return or disposal instructions.
devices
openFDA · August 19, 2026Moderate risk
Terumo Medical Corporation : GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the…
Terumo Medical Corporation is recalling its Glidesheath Slender A-Kit 6F 10CM .021GW, product code 60-1060, used to guide catheters into the radial artery. The kit contains a 0.025 guidewire instead of the required 0.021 guidewire, which could lead to procedural complications for patients undergoing catheterization. Consumers should stop using the affected kits and contact Terumo or their distributor for return and replacement instructions.
devices
openFDA · August 19, 2026Moderate risk
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. : Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
Philips Medical Systems is recalling its Allura Xper FD interventional fluoroscopic x-ray systems, models 722026, 722027, 722028, 722029, 722035, 722038, 722039, and 722058. A firmware issue can cause loss of geometry movements, exposing patients and staff to potential harm during procedures. Users should contact Philips for instructions on correcting the firmware issue.
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO…
Cardinal Health Presource Kits, including neuro, cervical disc, and laminectomy procedure kits, are affected. The kits contain MEDICOM Ritmed Neurological Sponges with unexpected variability in endotoxin levels, exposing patients to risk. Consumers should stop using the recalled kits and follow the firm's instructions for return or disposal.
devices
openFDA · August 19, 2026Moderate risk
Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, product number MSC351450BG4, are recalled. The wipes may lose bleach strength before the 12-month shelf life ends, which can reduce disinfection and allow harmful germs to survive for users. Consumers should stop using the recalled wipes and contact Medline Industries for instructions.
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
Cardinal Health Presource Kits, specifically the Harmonized Spine VCH PHC Pack (catalog SOP30SPBCC), are affected. The kits contain Medicom Ritmed Neurological Sponges with unexpected variability in endotoxin levels, posing a risk to patients during procedures. Consumers should stop using the affected kits and contact Cardinal Health for return or disposal instructions.
devices
openFDA · August 19, 2026Moderate risk
MICROVENTION INC. : BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an…
Microvention Inc. is recalling its BOBBY Balloon Guide Catheter, models BOB-895-CN, BOB-895-EMEA, BOB-895-EMEA-AL, BOB-895-US, and MV-BGA01095. The balloon may have pinhole defects, posing a risk to patients undergoing vascular procedures. Consumers should stop using the affected catheters and contact Microvention or their distributor for instructions.
devices
openFDA · August 19, 2026Moderate risk
Covidien, LP : V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE…
Covidien, LP is recalling its V-Loc 180 Absorbable Wound Closure Device. The sterile barrier packaging may have a perforation or tear, risking biocontamination of sutures and causing infection, vision loss, or prolonged surgery for patients. Consumers should stop using affected devices and contact Covidien or their healthcare provider for return instructions.
devices
openFDA · August 19, 2026Moderate risk
Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4)…
Cardinal Health Presource Kits, including ENT, sinus, nasal septoplasty, head and neck, nasal, and EENT trays with specific catalog numbers, are affected. The kits contain MEDICOM Ritmed Neurological Sponges with unexpected variability in endotoxin levels, exposing patients to potential harm. Consumers should stop using these kits and contact Cardinal Health for return or replacement instructions.
devices
openFDA · August 19, 2026Moderate risk
W L Gore & Associates, Inc. : GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…
The recall affects GORE VIABIL Biliary Endoprosthesis, Model VSWVN1010, distributed in Georgia and Rhode Island. The device is mislabeled, containing a 10 mm x 7 cm stent with drainage holes instead of the 10 mm x 10 cm version without holes,
devices
openFDA · August 19, 2026Moderate risk
Shoolin Pharma Chem LLP : TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near…
Shoolin Pharma Chem LLP is recalling TADALAFIL USP, a 1 kg bag of bulk drug ingredient for prescription compounding. The product may be contaminated or otherwise compromised due to manufacturing deviations, posing a risk to patients who receive compounded medications made with it. Consumers should contact their pharmacist or healthcare provider to determine if their medication is affected and seek a replacement.
drugs
openFDA · August 19, 2026Moderate risk
Shoolin Pharma Chem LLP : SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani…
Shoolin Pharma Chem LLP is recalling Sildenafil Citrate USP, a prescription compounding ingredient sold in 1.00 kg bags. The product may be affected by CGMP deviations found during an FDA inspection, posing a risk to patients who receive compounded medications made with it. Consumers should contact their pharmacist or healthcare provider to determine if their medication is affected and seek guidance.
drugs
openFDA · August 19, 2026High risk
Baxter Healthcare Corporation : Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only,…
Baxter Healthcare Corporation is recalling Cefazolin in Dextrose Injection, USP, 2g/100mL single-dose infusion bags. The product contains particulate matter, which poses a risk of serious harm to patients receiving the intravenous infusion. Consumers should stop using the recalled product and contact their healthcare provider or pharmacy for further instructions.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102,…
Apollo Care is recalling its Semaglutide 5mg (1mg/mL) and Glycine 25 mg (5mg/mL) sterile multi-dose vials for injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients. Consumers should stop using the recalled vials and contact their pharmacist or Apollo Care for return instructions.
drugs
openFDA · August 19, 2026Moderate risk
Novartis Pharmaceuticals Corporation : Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis…
Novartis is recalling Diovan (valsartan) 160 mg tablets, 90-count bottles, made by Patheon and distributed nationwide. The tablets fail dissolution specifications, so they may not dissolve properly and deliver the full dose, affecting patients who take this specific product. Consumers should check the lot number and return the recalled bottles to their pharmacy or contact Novartis for replacement.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…
Apollo Care is recalling Semaglutide 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vials for subcutaneous injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients nationwide. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for guidance.
drugs
openFDA · August 19, 2026Moderate risk
Shoolin Pharma Chem LLP : TADALAFIL USP, 0.500 KG, 0.500KG(500gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes,…
Shoolin Pharma Chem LLP is recalling Tadalafil USP, a prescription compounding ingredient sold in 0.5 kg bags. The product may be ineffective or unsafe due to manufacturing deviations, affecting patients who receive compounded medications made with it. Consumers should stop using any medication compounded with this ingredient and contact their pharmacist for a replacement.
drugs
openFDA · August 19, 2026Moderate risk
Shoolin Pharma Chem LLP : TADALAFIL USP, 0.100 KG, 0.1KG(100gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes,…
Shoolin Pharma Chem LLP is recalling Tadalafil USP, a bulk drug ingredient sold in 100-gram bags for prescription compounding. The product was made without proper manufacturing controls, posing a quality and safety risk to patients receiving compounded medications made with it. Consumers should contact their pharmacist or healthcare provider to check if their medicine contains this recalled ingredient and follow their guidance.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.…
Apollo Care is recalling Semaglutide 9mg (4.5 mg/mL) 2 mL sterile multi-dose vials for subcutaneous injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, which can harm patients who inject the drug. Consumers should stop using the recalled vials and contact Apollo Care or their pharmacy for return and replacement instructions.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…
Apollo Care is recalling semaglutide 10 mg (5 mg/mL) with glycine, 2 mL sterile multi-dose vials for injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients who inject the product. Consumers should stop using the recalled vials and contact their prescriber or pharmacy for guidance.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…
Apollo Care, LLC is recalling its Semaglutide 20mg (5mg/mL) with Glycine 20mg (5mg/mL) 4 mL sterile multi-dose vials, distributed nationwide. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous-type material, posing a risk to patients who inject the product. Consumers should stop using the recalled vials and contact their prescriber or pharmacy for guidance.
drugs
openFDA · August 19, 2026Moderate risk
Prestige Brands Holdings : CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer…
The recall affects CLEAR EYES Maximum Itchy Eye Relief 0.5 fl oz sterile eye drops, distributed by Medtech Products Inc. for Prestige Consumer Healthcare. The product may be contaminated, so using it poses a risk of eye infection to consumers nationwide. Consumers should stop using the recalled drops and return or discard them according to the recall notice.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…
Apollo Care, LLC is recalling Semaglutide 0.9 mg/mL sterile multi-dose vials for subcutaneous injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients who inject the product. Consumers should stop using the recalled vials and contact their prescriber or pharmacy for guidance.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…
Apollo Care, LLC is recalling Semaglutide 6.75mg (4.5 mg/mL) sterile multi-dose vials. The vials contain particulate matter (nylon/polyamide and silk/proteinaceous material), posing a risk to patients who inject the drug. Consumers should stop using the recalled vials and contact Apollo Care or their healthcare provider for guidance.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste…
Apollo Care is recalling its Semaglutide 2.5mg (1mg/mL) with Glycine 12.5 mg (5mg/mL) sterile multi-dose vials for subcutaneous injection. The vials contain particulate matter, nylon/polyamide and silk/proteinaceous material, posing a risk to patients who inject the drug. Consumers should stop using the recalled vials and return them to the pharmacy or contact Apollo Care.
drugs
openFDA · August 19, 2026Moderate risk
Heritage Pharmaceuticals Inc : CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816,…
Heritage Pharmaceuticals Inc. is recalling clindamycin palmitate hydrochloride for oral solution, 75 mg/5 mL, 100 mL, distributed by Avet Pharmaceuticals Inc. The hazard is the presence of particles and white flakes in the reconstituted bottles, posing a risk to patients taking this prescription antibiotic. Consumers should stop using the recalled product and consult their healthcare provider.
drugs
openFDA · August 19, 2026High risk
Liebel-Flarsheim Company LLC : Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution,…
Liebel-Flarsheim Company LLC is recalling Optiray Imaging Bulk Package-350 (ioversol injection 74%) in 500 mL vials. The vials may contain particulate matter such as polyethylene, plastic, stainless steel, and glass, posing a risk to patients receiving the injection. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for instructions.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…
Apollo Care, LLC is recalling its Semaglutide 2.25mg (0.9 mg/mL) sterile multi-dose vials sold under the Apollo Care brand. The vials contain particulate matter, including nylon/polyamide and silk/proteinaceous material, posing a risk to patients who inject the drug. Consumers should stop using the recalled vials and contact Apollo Care or their pharmacy for return instructions.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…
Apollo Care is recalling Semaglutide 12.5mg (2.5mg/mL), 5 mL sterile multi-dose vials for subcutaneous injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients nationwide. Consumers should stop using the recalled vials and contact Apollo Care or their pharmacist for instructions.
drugs
openFDA · August 19, 2026High risk
Victory Medical Center Pharmacy : Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile…
Victory Medical Center Pharmacy is recalling Glutathione (MDV) 200 mg/mL, 30 mL vials. The sterile injection may contain bacterial endotoxin, posing infection risk to patients who use it. Consumers should stop using the product and return it to the pharmacy or contact their healthcare provider.
drugs
openFDA · August 19, 2026Moderate risk
Apollo Care, LLC : SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…
Apollo Care, LLC is recalling semaglutide 7.5 mg (5 mg/mL) with glycine 7.5 mg (5 mg/mL) in 1.5 mL sterile multi-dose vials for subcutaneous injection. The vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material, posing a risk to patients who inject the drug. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacist for instructions.
drugs
openFDA · August 19, 2026Moderate risk
Shoolin Pharma Chem LLP : SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani…
The recall affects Sildenafil Citrate USP, 100 gm bags, from Shoolin Pharma Chem LLP, distributed nationwide in the USA. The hazard is CGMP deviations found during an FDA inspection, exposing patients who receive compounded prescriptions made with this ingredient. Consumers should stop using the product and contact their pharmacist or prescriber for return and guidance.
drugs
openFDA · August 19, 2026High risk
Buy-Herbal : Kian Pee Wan Capsules, 30-count bottles
Buy-Herbal brand Kian Pee Wan Capsules, 30-count bottles, are recalled. The capsules contain undeclared dexamethasone and cyproheptadine, posing risks to consumers who bought them from an eBay third-party seller. Consumers should stop using the product and return it to the seller or discard it.
drugs
openFDA · August 19, 2026High risk
Taylor Farms de Mexico S. de R.L. de C.V. : SYSCO LETTUCE SALAD MIX 4/5# SYSCO LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.
Taylor Farms de Mexico's Sysco lettuce salad mix, including the 4/5# lettuce salad and 4/5# lettuce salad with separate bag, is recalled. The salads may contain Cyclospora, a parasite that can cause serious intestinal illness, and were distributed in many US states and Mexico. Consumers who bought these Sysco salads should not eat them and should discard or return them for a refund.
food

Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.

Recalls & alerts

W L Gore & Associates, Inc. : GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1006. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB

Straumann USA LLC : Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form

Covidien, LP : V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12…

Erbe USA Inc : ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. : Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 and R3.1;…

Remel Europe Ltd. : Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics

Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI…

Ventana Medical Systems, Inc. : navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code:…

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD , Catalog Number: 21-4720C; 3) KIT,BOSC…

Covidien, LP : Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX

Galt Medical Corporation : Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/…

Baxter Healthcare Corporation : Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets

Spectra Medical Devices, Llc : Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride…

Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN

Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN

Terumo Medical Corporation : GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. : Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO…

Medline Industries, LP : Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC

MICROVENTION INC. : BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an…

Covidien, LP : V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE…

Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4)…

W L Gore & Associates, Inc. : GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…

Shoolin Pharma Chem LLP : TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near…

Shoolin Pharma Chem LLP : SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani…

Baxter Healthcare Corporation : Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only,…

Apollo Care, LLC : SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102,…

Novartis Pharmaceuticals Corporation : Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis…

Apollo Care, LLC : SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…

Shoolin Pharma Chem LLP : TADALAFIL USP, 0.500 KG, 0.500KG(500gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes,…

Shoolin Pharma Chem LLP : TADALAFIL USP, 0.100 KG, 0.1KG(100gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes,…

Apollo Care, LLC : SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.…

Apollo Care, LLC : SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…

Apollo Care, LLC : SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…

Prestige Brands Holdings : CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer…

Apollo Care, LLC : SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…

Apollo Care, LLC : SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…

Apollo Care, LLC : SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste…

Heritage Pharmaceuticals Inc : CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816,…

Liebel-Flarsheim Company LLC : Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution,…

Apollo Care, LLC : SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…

Apollo Care, LLC : SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO…

Victory Medical Center Pharmacy : Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile…

Apollo Care, LLC : SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…

Shoolin Pharma Chem LLP : SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani…

Buy-Herbal : Kian Pee Wan Capsules, 30-count bottles

Taylor Farms de Mexico S. de R.L. de C.V. : SYSCO LETTUCE SALAD MIX 4/5# SYSCO LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.