Recalls & alerts

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

• openFDA · August 26, 2026Moderate risk

  American Regent, Inc. : ACETYLCYSTEINE SOLUTION, USP, 10% (100 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7504-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC…

  American Regent, Inc. is recalling Acetylcysteine Solution, USP, 10% (100 mg/mL) in 4 mL and 25x4 mL vials labeled NOT FOR INJECTION. The solution may contain particulate matter including hair, glass, and paraformaldehyde, posing a risk to patients who use it. Consumers should stop using the recalled product and contact American Regent for return instructions.

  drugs
• openFDA · August 26, 2026High risk

  American Regent, Inc. : Papaverine HCl Injection, USP, 60 mg/2 mL (30 mg/mL), packaged in a) 2mL Single-Dose Vial (NDC 0517-4002-01), and b) 25x2mL Single-Dose Vials (NDC…

  American Regent, Inc. is recalling Papaverine HCl Injection, USP, 60 mg/2 mL (30 mg/mL) single-dose vials. The injection contains glass and/or paraformaldehyde particulate matter, posing a risk to patients who receive it. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacist for instructions.

  drugs
• openFDA · August 26, 2026Moderate risk

  American Regent, Inc. : ACETYLCYSTEINE SOLUTION, USP, 20% (200 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7604-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC…

  American Regent, Inc. is recalling Acetylcysteine Solution, USP, 20% (200 mg/mL) in 4 mL vials, sold as single vials and 25-vial packs. The solution may contain particulate matter including hair, glass, or paraformaldehyde, posing a risk to patients who use it. Consumers should stop using the recalled vials and return them to the pharmacy or contact American Regent for a refund or replacement.

  drugs
• openFDA · August 26, 2026Moderate risk

  American Regent, Inc. : Multrys (Trace Elements Injection 4, USP), For intravenous infusion, packaged in a) 1 mL Single-Dose Vial (NDC 0517-9302-01), and b) 25x1 mL Single-Dose Vials…

  American Regent, Inc. is recalling Multrys (Trace Elements Injection 4, USP) 1 mL single-dose vials. The product contains particulate matter such as hair, glass, or paraformaldehyde, posing a risk to patients receiving intravenous infusion. Consumers should stop using the recalled vials and contact their pharmacist or healthcare provider for further instructions.

  drugs
• openFDA · August 26, 2026Moderate risk

  Golden State Medical Supply Inc. : Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC 51407-215-01), Rx Only, Manufactured by: Taro…

  Golden State Medical Supply Inc. is recalling Carbamazepine Tablets, USP, 200mg, in 100-count and 1000-count bottles. The tablets may contain black specks, posing a risk to patients taking this prescription drug. Consumers should stop using the recalled tablets and return them to their pharmacy or contact their healthcare provider.

  drugs
• openFDA · August 26, 2026Moderate risk

  American Regent, Inc. : Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial (NDC 0517-0032-01) and b) 25x10 mL…

  American Regent, Inc. is recalling Cyanocobalamin injection USP, 10,000 mcg/10 mL, packaged in 10 mL multi-dose vials. The product may contain particulate matter such as hair, glass, or paraformaldehyde, posing a risk to patients who receive the injection. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for instructions.

  drugs
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Mango Pineapple Salsa sold as a condiment in Caribbean Mango Pineapple Turkey Burger. Keep Refrigerated. Packed in various sized clear plastic…

  Whole Foods Mango Pineapple Salsa, sold as a condiment with Caribbean Mango Pineapple Turkey Burger, is recalled. The salsa may be contaminated with Salmonella, posing a risk to consumers who purchased it. Consumers should not eat the product and should return or discard it.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Salsa, Heirloom Tomato. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is…

  Whole Foods Market's Heirloom Tomato Salsa, sold in clear plastic containers, is affected. The salsa may be contaminated with Salmonella from jalapenos, posing a risk to consumers who eat it. Consumers should not eat the product and should return it to the place of purchase.

  food
• openFDA · August 26, 2026High risk

  Coast Citrus Distributors : Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9…

  Coast Citrus Distributors is recalling Jalapeno Peppers in bulk Coast Tropical cardboard packaging. The peppers may be contaminated with Salmonella Javiana, posing a risk to consumers and food processors who handle them. Consumers who have the product should not eat it and should return or discard it.

  food
• openFDA · August 26, 2026High risk

  GET FRESH PRODUCE : Get Fresh Produce Jalapeno Peppers. Item 01896 - 2 lb. box; Item 01894 - 10 lb. box

  Get Fresh Produce Jalapeno Peppers in 2 lb and 10 lb boxes are recalled. The peppers may contain Salmonella, which can cause serious illness, and were sold in Illinois, Indiana, Michigan, and Wisconsin. Consumers who bought them should not eat them and should return or discard them.

  food
• openFDA · August 26, 2026High risk

  Lidl US TRADING : VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY LIDL US, LLC ARLINGTON, VA 22202 PRODUCT OF THE CZECH REPUBLIC

  Lidl US is recalling VITASIA Asian Style Wok Spice Mix in 1.58 oz packages. The product may be contaminated with Salmonella, which can cause serious illness, especially in vulnerable people. Consumers who bought this spice mix should not eat it and should return it to the store or throw it away.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Trio Dip, Contains Pico de Gallo, Guacamole, Salsa. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a…

  Whole Foods Trio Dip, sold under the Whole Foods Market brand, is affected. The dip may contain Salmonella from jalapenos, posing a risk to anyone who eats it. Consumers should throw it away or return it to the store for a refund.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Mild Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is…

  Whole Foods Market recalls its Mild Guacamole Dip packed in clear plastic containers. The dip may contain Salmonella from jalapenos, posing a risk to anyone who eats it. Consumers should not eat the product and should return it to the store or throw it away.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Roasted Corn Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is…

  The recalled product is Whole Foods Roasted Corn Guacamole Dip in clear plastic containers. The dip may contain Salmonella from jalapenos, posing a risk to anyone who eats it. Consumers should not eat the dip and should return it to the store or throw it away.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Spicy Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product…

  Whole Foods Market is recalling its Spicy Guacamole Dip No Tomatoes, packed in various sized clear plastic containers. The dip may be contaminated with Salmonella from jalapenos, posing a health risk to anyone who consumes it. Consumers should not eat the product and should return it to the store for a refund.

  food
• openFDA · August 26, 2026High risk

  Publix Super Markets, Inc. : Organic Whole Blueberries, Net Wt. 48 oz (3Lb) plastic bag, packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12053

  Publix Super Markets, Inc. is recalling its Organic Whole Blueberries in 48-ounce plastic bags. The frozen berries may be contaminated with E. coli O145:H28, affecting consumers in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia. Consumers should not eat them and should return or discard the product.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Mild Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product…

  Whole Foods Market's Mild Guacamole Dip No Tomatoes, Keep Refrigerated, packed in various clear plastic containers, is affected. The product may contain Salmonella from jalapenos, posing a risk to consumers in AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX, and WI. Consumers should not eat the product and should discard it.

  food
• openFDA · August 26, 2026High risk

  Dairyland Produce, LLC : Dairyland Produce, LLC Pepper Jalapeno, repackaged into the following sized clear plastic bags: 1. 1 lb., item number 01213, UPC 0009907729 2. 3 lbs., item…

  Dairyland Produce, LLC Pepper Jalapeno in clear plastic bags of 1, 3, 5, and 10 pounds is affected. The jalapenos may be contaminated with Salmonella, affecting consumers in Louisiana and Texas. Consumers should check the recalled item numbers and UPCs for the product.

  food
• openFDA · August 26, 2026Moderate risk

  Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc. : Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz. UPC 733163001576, product is sold at grocery stores with paper…

  Grand Central Bakery's Potato Sourdough Bread, sold as Potato Market Loaf, Potato Table Loaf, and Mini Potato Loaf, is affected. The bread may contain metal pieces, posing a risk to consumers in Washington state. Consumers should not eat the recalled bread and should return it to the store or throw it away.

  food
• openFDA · August 26, 2026High risk

  Publix Super Markets, Inc. : Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen UPC 41415-06453

  Publix Super Markets, Inc. is recalling its Organic Whole Blueberries in 10 oz plastic bags with UPC 41415-06453. The blueberries may be contaminated with E. coli O145:H28, posing a serious health risk to consumers in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia. Consumers should not eat the product and should return it to the store or throw it away.

  food
• openFDA · August 26, 2026Low risk

  Prospector Popcorn, LLC : Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz

  Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn in 3.5oz packages is recalled by Prospector Popcorn, LLC. The labels understate iron and overstate vitamin D, which misleads consumers about nutrient content. Consumers should return the product to the store or discard it.

  food
• openFDA · August 26, 2026Moderate risk

  Prospector Popcorn, LLC : Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.

  Prospector Popcorn Chocolate Mocha Gourmet Popcorn in 1.5 oz. packages is recalled by Prospector Popcorn, LLC. The product has inaccurate nutrition labels that understate carbohydrate and cholesterol levels, exposing consumers to misleading dietary information. Consumers who bought this popcorn should not eat it and should return or discard it.

  food
• openFDA · August 26, 2026High risk

  Publix Super Markets, Inc. : Organic Whole Mixed Berries, Net Wt. 10 oz (284 g) plastic bags, packed in 8 bags per case of 10 oz each. Keep Frozen. UPC 41415-06753

  Publix Super Markets, Inc. is recalling its Organic Whole Mixed Berries in 10 oz plastic bags with UPC 41415-06753. The berries may be contaminated with E. coli O145:H28, posing a serious health risk to consumers who purchased them in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia. Consumers should not eat the recalled berries and should return them to the store or throw them away.

  food
• openFDA · August 26, 2026Moderate risk

  Gifford's Dairy, Inc. : Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7

  Gifford's HomeMaine ice cream brand Power Play Fudge, one quart (946 mL) with UPC 8 60864 00030 7, is recalled. The ice cream may contain rubber pieces, posing a choking or injury hazard to consumers in Massachusetts, Maine, and Vermont. Consumers should not eat the product and should return it to the store or discard it.

  food
• openFDA · August 26, 2026Low risk

  Prospector Popcorn, LLC : Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

  Prospector Popcorn, LLC is recalling its Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn in 3.5 oz packages. The product has inaccurate nutrient labels, with potassium and calcium overstated and iron understated, affecting consumers who purchased it. Consumers should return or discard the recalled popcorn.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is…

  Whole Foods Pomegranate Guacamole Dip, sold in clear plastic containers, is affected. The dip may contain Salmonella from jalapenos, posing a risk to anyone who eats it. Consumers should not eat the dip and should return it to the store or discard it.

  food
• openFDA · August 26, 2026Moderate risk

  Nutrient Foods, LLC : Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow pouch. Net wt.8.9 oz (252g). 1 pillow pouch…

  Nutrient Foods, LLC is recalling its Protein Cereal Cocoa Crunch, a ready-to-eat cereal in an 8.9 oz pouch. The product contains undeclared soy, posing a risk to people with soy allergies. Consumers who have this cereal should not eat it and should return or discard it.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Spicy Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is…

  Whole Foods Spicy Guacamole Dip in clear plastic containers is recalled. The dip may contain Salmonella from jalapenos, posing a risk to consumers in AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX, and WI. Consumers should not eat the product and should return it to the store or discard it.

  food
• openFDA · August 26, 2026High risk

  Publix Super Markets, Inc. : Organic Whole Mixed Berries, Net Wt. 48 oz (3Lb) plastic bag. packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12153

  Publix Super Markets is recalling its Organic Whole Mixed Berries in 48-ounce plastic bags. The berries may be contaminated with E. coli O145:H28, posing a serious health risk to consumers who purchased them. Consumers should not eat the product and should discard it or return it to the store for a refund.

  food
• openFDA · August 26, 2026Low risk

  Prospector Popcorn, LLC : Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz

  Prospector Popcorn's Fudge Brownie Gourmet Popcorn in 1.5oz and 3.5oz packages is recalled. The labels overstate potassium and calcium, which is a hazard for consumers who eat this popcorn. Consumers should return the product to the place of purchase or contact Prospector Popcorn for a refund.

  food
• openFDA · August 26, 2026High risk

  WFM Purchasing, LP : Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product…

  Whole Foods Medium Pico de Gallo Guacamole Dip is affected, packed in clear plastic containers with PLU code 29802800000. The dip may contain Salmonella from jalapenos, posing a risk of serious infection to anyone who eats it. Consumers should not eat the product and should return it to the store or throw it away.

  food
• 

  CPSC · August 20, 2026High risk

  Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards

  Workbless electric pressure washers, models WB0301 and WB0302, are recalled. They lack an integral ground-fault circuit-interrupter and an adequate-length power cord, posing shock and electrocution hazards to users. Consumers should stop using the recalled pressure washers immediately.

  Photo: CPSC

  consumer-product
• 

  CPSC · August 20, 2026High risk

  Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard

  The recall affects Airedale ventilation fans in ClassMate and SchoolMate heat pumps used in classrooms and schools. The fan motor can short circuit if water gets on the circuit board, causing overheating and a fire hazard for students and staff. Consumers should check the brand sticker and serial plate to identify affected units.

  Photo: CPSC

  consumer-product
• 

  CPSC · August 20, 2026High risk

  KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard

  KTM North America is recalling certain 2021-2024 GASGAS and Husqvarna off-road motorcycles. The rear brake caliper can crack or break, reducing braking effectiveness and posing a crash hazard to riders. Consumers should stop using the recalled motorcycles and contact KTM North America for a free repair.

  Photo: CPSC

  consumer-product
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  CPSC · August 20, 2026High risk

  Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology

  The recalled product is the Koorlian brand 10-inch Twin XL mattress, sold on Amazon by Dream Bedding Technology. The mattresses violate the mandatory flammability standard, posing a risk of serious injury or death from fire to consumers. Consumers must stop using the recalled mattresses.

  Photo: CPSC

  consumer-product
• 

  CPSC · August 20, 2026High risk

  JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO

  The recall involves JINHEZO Mini Waterproof LED Tea Lights, imported by Mystic ZO. The button cell batteries can be easily accessed by children, posing an ingestion hazard that can cause serious injury or death. Consumers must ensure children cannot access the batteries in these recalled tea lights.

  Photo: CPSC

  consumer-product
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  CPSC · August 20, 2026High risk

  Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards

  Goal Zero recalls its YETI 3000X portable power stations. The circuit board can overheat, posing fire and burn hazards to consumers. Consumers should stop using the recalled power stations immediately.

  Photo: CPSC

  consumer-product
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  CPSC · August 20, 2026High risk

  CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards

  CCM Hockey U.S. recalled FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories. The visors can crack upon impact, posing laceration or impact injury risk to hockey players. Consumers should check the serial number on their visor to see if it matches the recalled list.

  Photo: CPSC

  consumer-product
• openFDA · August 19, 2026Moderate risk

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. : Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 722225, 722226, 722227, 722228, 722280*,…

  Philips is recalling its Azurion Rystem interventional fluoroscopic X-ray systems with software versions R2.2.10 and R2.1.10. Two software issues can degrade image quality or cause loss of geometry movements, leading to delayed therapy, procedural complications, or inappropriate treatment for patients. The voluntary, firm-initiated recall requires users to contact Philips for corrective action.

  devices
• openFDA · August 19, 2026Moderate risk

  BioFire Diagnostics, LLC : BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic

  BioFire Diagnostics, LLC is recalling its BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 test. The test may give false negative results, affecting patients tested in Alabama, Arkansas, Iowa, Illinois, Kansas, Louisiana, Minnesota, Missouri, Texas, and Wisconsin. Consumers should contact their healthcare provider for guidance on next steps.

  devices
• openFDA · August 19, 2026Moderate risk

  OBP Medical Corporation : OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

  OBP Medical is recalling its ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF C020130-1. The device may contain a burr on the proximal plastic blade, posing a sharp-edge injury risk to patients and healthcare providers. Consumers should stop using the recalled speculum and contact OBP Medical for return and replacement.

  devices
• openFDA · August 19, 2026Moderate risk

  Covidien, LP : Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31

  Covidien, LP is recalling Dermalon 4-0 blue 75cm sutures with catalog numbers 88861757-31 and 88861799-31. The sterile packaging may have a tear or perforation, allowing contamination that could cause infection, vision loss in eye surgery, or longer surgery for patients. Consumers and healthcare providers should stop using affected sutures, check inventory, and contact Covidien for return instructions.

  devices
• openFDA · August 19, 2026Moderate risk

  Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number:…

  Cardinal Health Presource Kits, including Basic Pack, Spine Pack, and Craniotomy Pack 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 the recalled kits and contact Cardinal Health for return and replacement instructions.

  devices
• openFDA · August 19, 2026Moderate risk

  Covidien, LP : Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623

  Covidien, LP is recalling its Surgipro SP-623 SURGIPRO 2-0 BLU 75CM SC2 X36 SP-623 sutures. The sterile barrier packaging may have a perforation or tear, causing biocontamination that can lead to infection, vision loss in ophthalmic use, or prolonged surgery for patients. Consumers should stop using the affected sutures and contact Covidien, LP for instructions.

  devices
• openFDA · August 19, 2026Moderate risk

  Bioporto Diagnostics A/S : ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.

  The affected product is the ProNephro AKI (NGAL) Reagent Kit by Bioporto Diagnostics. A non-validated rework process could lead to missed diagnosis or inappropriate treatment of renal disease in patients. Consumers should contact Bioporto Diagnostics for instructions on the recalled product.

  devices
• openFDA · August 19, 2026Moderate risk

  Straumann USA LLC : GM Helix Implant, Endosseous Dental Implant Article No. 109.984

  Straumann USA LLC is recalling its GM Helix Implant, Endosseous Dental Implant Article No. 109.984. The implant inside the packaging may not match the label, which could cause bone compression or difficulty during installation for patients. Consumers should verify the implant matches the label before use.

  devices
• openFDA · August 19, 2026Moderate risk

  Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2…

  Cardinal Health Presource Kits, including Septo Rhino Pack, Neuro Minor Craniotomy, and other neurological and spine packs, 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

  Waldemar Link GmbH & Co. KG (Mfg Site) : Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16

  Waldemar Link GmbH & Co. KG is recalling its Endo-Model Replacement Set Tibial Plateau, item number 15-0027/16. The set incorrectly contains a Pure Hinge plateau, which can cause prolonged surgery or, if implanted, increased wear and reduced implant life for patients. Consumers should contact their healthcare provider or the firm to arrange return of the affected product.

  devices
• openFDA · August 19, 2026Moderate risk

  BD SWITZERLAND SARL : 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619…

  BD Switzerland SARL is recalling its 60-inch Non-DEHP Minibore Extension Set, MaxPlus Ext Set with Needleless and Y-Site, and 9-inch Extension Set with Max Y. The devices may not have received adequate sterilization, posing infection risk to patients who receive fluids through them. Consumers should stop using affected products and contact BD or their healthcare provider for return instructions.

  devices
• openFDA · August 19, 2026Moderate risk

  Spacelabs Healthcare, Inc. : Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare…

  Spacelabs Healthcare's Xhibit Central Station, model 96102, is affected. The DisplayPort audio/video splitter can fail, causing loss of patient data on external monitors, affecting clinicians and patients. Users should contact Spacelabs Healthcare for instructions.

  devices

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