1084 alerts recorded, refreshed every six hours. Filter by source or category.
Baxter Healthcare Corporation is recalling Dextrose Injection, USP, 70%, 2000 mL bags, a prescription drug. The solution contains stainless steel particles, posing a hazard to patients who receive the injection. Consumers should stop using the affected product and contact their healthcare provider.
Ajanta Pharma USA Inc. is recalling Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles. The tablets failed impurity specifications, exposing patients to a slightly higher level of impurity-A. Consumers should check their bottles and contact their pharmacist or doctor for instructions.
ImprimisRx NJ LLC is recalling Povidone Iodine 1.25% and Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL dropper bottles, distributed nationwide. The product is subpotent, meaning it may not work as intended, exposing patients to inadequate disinfection or anesthesia during eye procedures. Consumers should stop using the recalled solution and return it to the place of purchase or contact the company for a refund.
Ferrero USA is recalling Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz. The product contains undeclared milk and pecans, which can cause serious reactions in people with allergies, and was sold in Iowa, Illinois, Indiana, and Ohio. Consumers who bought this product should not eat it and should return or discard it according to the recall notice.
International Specialty Supply alfalfa in 50-pound bags is recalled. The product may contain E. coli and Salmonella, posing a risk to anyone who eats it. Consumers should not eat the recalled alfalfa and should return it to the place of purchase.
Exotique Foods Canada is recalling Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower in 3oz packages with UPC 6 28634 44216 6. The chips contain undeclared wheat, posing a risk to people with a wheat allergy or celiac disease. Consumers who bought them should not eat the product and should return or discard it.
L-Nutra Inc is recalling Prolon Everyday Apulian Almond & Cocoa Spread in 8.47 oz glass jars. The product contains undeclared hazelnut, cashew, and pistachio, posing a risk to people with tree nut allergies. Consumers who bought it should stop using it and return or discard it according to the recall instructions.
Crown Farms Dried Suri Cut, 200 gram plastic packs, is recalled. The dried ribbon fish was not properly eviscerated, which can cause serious illness in consumers in VA, NY, NJ, and MI. Consumers should not eat it and should return or discard the product.
ZMC Group's battery-operated light-up toys, including a Mexican flag foam stick, unicorn headband, jelly rings, and heart balloon flower, are affected. The toys have easily accessible button cell batteries that can cause internal chemical burns or death if swallowed by children. Consumers should stop using the recalled toys and contact ZMC Group for instructions.
Victgoal recalls its red bicycle helmets, model HT-006, in size small, made in November 2025. The helmets fail the mandatory safety standard for retention and stability, so they may not protect users in a crash, risking serious head injury or death. Consumers should stop using the recalled helmets.
The recall affects 2025 and 2026 Triumph TF450 closed course competition motorcycles. The engine rocker arm can seize or stick, causing exhaust valves to stay open or break, which poses a crash hazard and risk of serious injury or death to riders. Consumers should check if their VIN is included at the Triumph recall website.
Sweet Cubby is recalling all children's loungewear sets, which are two-piece short-sleeved shirts and matching shorts in sizes 5-6Y through 13-14Y. The sets violate the mandatory flammability standard for children's sleepwear, posing a risk of serious burn injuries or death to children. Consumers should immediately stop using the recalled loungewear sets and keep them away from children.
The recall affects Lontcs Busy Board toys, which are wooden boards with various attached components. The zipper on the toys contains lead above the federal lead paint ban, posing a poisoning risk to young children who ingest it. Consumers should immediately stop using the recalled toys and keep them away from children.
Ricky Joy recalled more than 2.3 million Sour Crush Rolling Liquid Candy bottles. The rolling ball can detach, posing a choking hazard that can cause serious injury or death to consumers. Consumers should stop using the recalled bottles.
The recall involves Prepared Hero Hero Fire Spray Canisters, red and blue or red with the HERO Fire Spray logo, containing 20 fluid ounces. The canisters can deteriorate over time, rupture, and fail to operate during a fire, posing a risk of serious injury or death to consumers. Consumers should stop using the recalled canisters and check the date code 09/2024 on the base to determine if they are affected.
The recall involves DHASUWT Hair Dryer and Blow Dryer Brushes, model XR-8801, sold by Junkins. The hair dryers lack an immersion protection device, posing electrocution, shock, smoking, and fire hazards to consumers if they fall into water while plugged in. Consumers should immediately stop using the recalled hair dryers and contact Junkins for a refund or replacement.
The recall affects Wantefully 2 in 1 Hair Dryer & Styler brushes, model XR-8801. These hair dryers lack required immersion protection, posing electrocution, shock, and burn hazards to consumers if they fall into water or overheat. Consumers should immediately stop using them and contact Guang Zhou for a refund.
The recall affects FJTJBSI six-drawer wood dressers in black or white. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can cause serious injury or death to children. Consumers should stop using the recalled dressers.
The recall involves AGA Elise and Mercury Series and La Cornue CornuFé Series dual fuel ranges. A missing cap on the gas test port can cause a gas leak, posing fire or explosion hazards to anyone using the range. Consumers should stop using the recalled ranges immediately and contact AGA Rangemaster for a free repair.
The recalled product is the Cade California Electronic Finger Light toy, sold in boxes of 50 in white, blue, red and green. The toy's button cell batteries are easily accessible, and if swallowed by children, can cause internal chemical burns or death. Consumers should immediately stop using these finger lights and keep them away from children.
Golden State Medical Supply Inc. is recalling Prasugrel HCI Tablets, USP, 10mg, 30-count bottles. The tablets failed dissolution specifications, meaning they may not dissolve properly and could be less effective for patients taking this prescription drug. Consumers should stop using the recalled tablets and return them to the pharmacy or place of purchase.
Mylan Pharmaceuticals Inc. is recalling Prasugrel Tablets, USP, 10mg, 30-count bottles, distributed nationwide in the U.S. The hazard is that the product failed dissolution specifications and 18-month stability testing. Consumers should follow the recall instructions from Mylan or the FDA.
Chiesi USA, Inc. is recalling Revcovi (elapegademase-lvlr) Injection, 2.4mg/1.5mL, single-dose vials. The product failed stability specifications for its protein concentration profile, posing a hazard to patients who use it. Consumers should stop using the recalled product.
Sage Products LLC is recalling its 2% Chlorhexidine Gluconate Cloth, Non-sterile, 6 Disposable cloths. The hazard is cross contamination with other products, affecting consumers nationwide. Consumers should check the FDA recall notice for instructions.
Baxter Healthcare Corporation is recalling 0.9% Sodium Chloride Injection USP 500 mL in VIAFLEX Plastic Containers. The solution contains fiberglass particulate matter, posing a risk of injury to patients receiving the IV. Consumers should stop using the affected product and contact their healthcare provider for guidance.
American Health Packaging is recalling Buprenorphine Sublingual Tablets (C-III), 2 mg, 30-count cartons. The label mix-up poses a risk to patients who may receive the wrong medication. Consumers should stop using the affected product and contact their pharmacy or American Health Packaging for return instructions.
Optimal Balance Pharmacy is recalling Glutathione 200 mg/mL, 30 mL sterile multidose vials for injection. The vials may contain bacterial endotoxins, posing a risk of serious infection to patients who receive the injection. Consumers should stop using the recalled vials and contact their healthcare provider or pharmacy for guidance.
Medline Industries is recalling its Convenience Kits, including blood draw, phlebotomy, and blood culture kits. The kits' sterile packaging may be compromised by wrinkles in the paper lidding, exposing patients and users to microbial contamination. Consumers should consult the FDA recall notice for instructions.
Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays, with multiple catalog numbers affected. The wipes may be contaminated with a lubricant, causing localized skin irritation, erythema, or mild inflammation in patients. Consumers should check the recall notice for affected catalog numbers and follow the manufacturer's instructions.
Medline Industries recalled its Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, sold as PAIN PRE OP KIT DYKS1476A. The applicator packaging may have an open or incomplete seal, exposing patients to risk of skin, soft tissue, or systemic infection. Consumers should stop using the affected kits and contact Medline for instructions on returning the product.
Medline Industries is recalling three Convenience Kits: ORTHO ASPIRATION KIT DYKM1636A, SHOULD BLOCK KIT DYKM1881A, and TRIMA KIT DYNDB3077C. The kits contain applicators whose packaging may have wrinkles that break the sterile seal, exposing patients and users to microbial contamination and possible infection. Consumers should stop using the recalled kits and contact Medline Industries for instructions on returning or replacing them.
AVID Medical is recalling numerous surgical kits containing Medicom Ritmed Neurological Sponges, non-sterile models 55992C to 55998C. The sponges may have unexpected variability in endotoxin levels, posing a risk to patients during surgical procedures. Consumers should stop using affected kits, check the recall notice for specific lots, and contact AVID Medical for instructions.
Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays, catalog number PBOCGLN17. The wipes may be contaminated with a lubricant, which can cause skin irritation, erythema, or mild inflammation in patients. Consumers should stop using the affected product and follow the recall instructions.
Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes inside BD Urinary Catheter Trays, specifically the KIT, LUNG TX CIRCULATOR with catalog number OVC3507231. The wipes may be contaminated with a manufacturing lubricant, which can cause localized skin irritation, redness, or mild inflammation in patients. Consumers should stop using the affected wipes and contact Cardinal Health for further instructions.
Boston Scientific is recalling its LUX-Dx, LUX-Dx II, and LUX-Dx II+ Insertable Cardiac Monitor System server software, model 7246, all versions. The software may delay AF Burden Alert notifications, which could delay clinical evaluation or treatment for patients with atrial arrhythmias. Consumers should contact their healthcare provider or Boston Scientific for instructions on how to proceed.
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators are affected. The hazard is an open or incomplete seal on the applicator packaging, which may lead to infection in patients using the kits. Consumers should stop using the affected kits and contact Medline for instructions.
Boston Scientific's LUX-Dx, LUX-Dx II, and LUX-Dx II+ Insertable Cardiac Monitor System with server software model 7248 is affected. The software may delay AF Burden Alert notifications, which could delay clinical evaluation or treatment for patients with atrial arrhythmias. Consumers should contact their healthcare provider to discuss the recall and any needed follow-up.
Medline Industries, LP is recalling its Arterial Line Insertion Kit, model ART1295, part of its Convenience Kits. The kits contain applicators with a potential sterility breach due to wrinkles in the paper lidding, exposing patients and users to microbial contamination that could cause infection. Consumers should stop using the affected kit and contact Medline Industries for instructions.
Medline Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, C-SECTION PREP DYNJ32702B, are affected. The applicator packaging may have an open or incomplete seal, risking infection for users. Consumers should stop using affected kits and contact Medline for return or replacement.
Philips Brilliance CT systems, including models iCT, iCT Upgrades, and iCT SP with software 4.1.10.x, are affected. The systems have an unintended radiation issue that could affect equipment performance, exposing patients to potential risk. Consumers should contact their healthcare provider or Philips for instructions on what to do.
Medline Industries is recalling its Convenience Kit COLORECTAL ME, model DYNJ906437D. The kit's sterile packaging may have wrinkles that allow microbial contamination, exposing patients and users to possible infection. Consumers should stop using the affected kits and contact Medline Industries for instructions.
B Braun Medical Inc is recalling its Extension Set, the Discofix Four Way Stopcock, model 456025. The hazard is an incorrect expiration date printed on the carton shipper label, exposing users to potentially expired products. Consumers should check if their product is affected and follow the recall instructions from B Braun.
Fresenius Medical Care is recalling its 5008X HD/HDF with CLiC Blood Tubing Set, part number 03-5300-3C. A blood leak can occur at the connection between the Arterial Alpha Clip and the main line or pump segment, risking blood loss and hypovolemia for patients during dialysis. Consumers should check the part number and contact Fresenius or their dialysis provider for instructions.
Medline Industries is recalling Medline Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, specifically the Ortho Aspiration Kit DYKM1636A. The applicator packaging may have an open or incomplete seal, risking contamination and causing skin, soft tissue, or systemic infections for patients using the kits. Consumers should stop using the affected kits and contact Medline for instructions on return or replacement.
Medline Industries is recalling its Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, specifically the Blood Culture Kit 2 with Connect DYNDH1487A. The applicator packaging may have an open or incomplete seal, potentially causing contamination that can lead to skin, soft tissue, or systemic infections in users. Consumers should stop using the affected kits and contact Medline Industries for instructions.
Cardinal Health's Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays are affected, with catalog numbers PGOCRDNHD, PG36RPEAB, and PVCGVTACF. The wipes may be contaminated with a lubricant, causing skin irritation, erythema, or mild inflammation in patients. Consumers should check for the affected catalog numbers and follow the voluntary recall initiated by the firm.
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators, including specific pre-op kit models, are affected. The applicator packaging may have an open or incomplete seal, exposing patients to potentially contaminated applicators that can cause skin, soft tissue, or systemic infections. Consumers should stop using affected kits and follow the recall instructions from Medline.
Medline Industries is recalling several Medline Convenience Kits, including PRE-OP and GENERAL PREOP kits with specific catalog numbers. The kits contain applicators with a potential breach of sterility, exposing patients and users to microbial contamination that could cause infection. Consumers should stop using the affected kits and contact Medline Industries for further instructions.
Medline Industries is recalling Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators, specifically BASIN PACK-LF DYNJ42828B and EYE BASIN TRAY-LF DYNJ42832B. The applicator packaging may have an open or incomplete seal, exposing users to potentially contaminated applicators that can cause skin, soft tissue, or systemic infections. Consumers should verify their kit's lot number and follow the firm's voluntary recall instructions.
Medline Convenience Kits containing BD ChloraPrep Clear 1mL Applicators, including patient admin kits DYKA1384B, DYKA1384C, and welcome kit DYKS1206D, are affected. The applicator packaging may have an open or incomplete seal, exposing patients to risk of skin, soft tissue, or systemic infection. Consumers should stop using affected kits and follow the recall instructions.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.