Archive
556 recalls were announced in March 2024.
Of the 556 recalls this month scored against our rubric, 4% are Critical, 27% are Severe.
Which agencies issued them
Chin Jung White Kimchi jars recalled due to undeclared fish allergen. Products distributed to supermarkets in California, Colorado, and Nevada may pose risk to consumers with fish allergies.
The Quaker Oats Co. is voluntarily recalling Gatorade Protein Bar Peanut Butter Chocolate with Best Before dates of Aug-02-24 and earlier due to potential Salmonella. The product was distributed nationally and internationally.
The Quaker Oats Co. is recalling Quaker Chewy Dipps Peanut Butter bars due to potential Salmonella contamination. The recall affects products with a Best Before date of Aug-02-24 or earlier.
The Quaker Oats Co. is recalling Frito-Lay Popped & Baked Chips variety packs for potential Salmonella contamination. Affected products have best-before dates of August 2, 2024 or earlier and were distributed nationally and internationally.
Reser's Amish Macaroni Salad is recalled because some containers have a mislabeled side label that does not declare wheat, which is an ingredient in the product. This poses a risk to people with wheat allergies.
The Quaker Oats Company is voluntarily recalling Quaker Big Chewy Bars Chocolate Chip due to potential Salmonella contamination. The product, distributed nationwide and internationally, affected millions of cases.
Quaker Chewy Dipps Chocolate Chip bars are being recalled nationwide due to potential Salmonella contamination. Affected products have a Best Before date of Aug-02-24 or earlier.
Quaker Simply Granola Oats, Honey & Almonds Cereal with Best Before dates of Aug-02-24 or earlier is being recalled due to potential Salmonella contamination. The voluntary recall affects 22,512,942 cases distributed nationwide.
The Quaker Oats Co. is recalling Cap n Crunch OOPS! All Berries Cereal (10.3 oz) due to potential Salmonella contamination. Products with a Best Before date of Aug-02-24 or earlier are affected nationally.
The Quaker Oats Co. is recalling Quaker Simply Granola Oats, Honey, Raisins & Almonds Cereal due to potential Salmonella. Affected products have Best Before dates of August 2, 2024, or earlier and were distributed nationally and internationally.
Frito-Lay has recalled Snack Time Favorites variety packs due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024 or earlier and were distributed nationally and internationally.
The Quaker Oats Company is voluntarily recalling Quaker Chewy Dipps Variety Pack snack bars due to potential Salmonella contamination. The recall affects products distributed nationally across all U.S. states, territories, and some international markets.
Quaker Oats is recalling Quaker Chewy Bars Less Sugar variety across multiple package sizes due to potential Salmonella contamination. The recall affects products distributed nationally and internationally with Best Before dates of August 2, 2024 or earlier.
Zingerman's Bakehouse is recalling Black Magic Brownie products due to undeclared walnut allergen. Affected consumers with walnut allergies should not consume the product.
The Quaker Oats Company is recalling Quaker Chewy Bars S'mores in multiple package sizes due to potential Salmonella contamination. The recall affects products distributed nationally and internationally.
The Quaker Oats Company is recalling Quaker Chewy Bars and Dipps Variety Packs due to potential Salmonella contamination. The affected products were distributed nationally and internationally, and consumers should discard or return them.
Sun Pharmaceutical is recalling Mesalamine extended-release capsules due to failed dissolution specifications. The affected capsules may not dissolve and release medication properly.
Equate Lubricant Eye Ointment, distributed nationwide by Walmart, is being recalled because the manufacturer cannot assure the product's sterility. The recall affects 315,842 units across multiple lots.
CVS Health Lubricant Eye Ointment is being recalled nationwide due to lack of sterility assurance during manufacturing. The recall affects 159,334 units distributed in 3.5-gram tubes with lot numbers A2F03, A2I02, A2L02, A3C04, and A3H04.
Seatex LLC is recalling 1,282 cases of 7 Eleven Hand Sanitizer Gel due to manufacturing facility deficiencies found during FDA inspection. The product was distributed nationwide.
Denver Solutions is recalling Lidocaine-Phenylephrine injectable vials nationwide due to glass delamination in the vials. The defect could potentially introduce glass fragments into the medication.
Denver Solutions is recalling Moxifloxacin PF eye injection vials nationwide due to glass delamination in the vials. The affected product is used for eye surgery injections.
Olympus is recalling 47 colonoscope units (Model PCF-H190DL) because they were assembled without protective adhesive. The missing adhesive may cause equipment failure under vibration, temperature changes, or shock.
Alphatec Spine recalls IdentiTi ALIF graft bolts after reports of breakage during implantation. Approximately 12,777 devices are affected worldwide.
Integra LifeSciences is recalling 161 units of the Cranial Access Kit (Lot 7124720) due to packaging defects that may compromise sterility. The recall affects units distributed worldwide.
Olympus Corporation is recalling 97 Colonoscope Model CF-HQ190L units distributed nationwide. The devices were assembled without protective adhesive, risking malfunction under vibration, temperature changes, or shock.
Integra LifeSciences is recalling the Cranial Access Kit due to a defect in the sterile packaging that may compromise product sterility. Affects 30 units distributed worldwide.
Integra LifeSciences is recalling 188 units of the Integra Cranial Access Kit because defective sterile packaging may have compromised product sterility.
Olympus is recalling 28 colonoscopes (Model PCF-HQ190L) due to missing adhesive that protects the device from vibration, temperature changes, and physical shock. The defect could cause device malfunction during procedures.
Integra LifeSciences is recalling the INS7280 Cranial Access Kit due to a packaging defect that may compromise product sterility. The recall affects 82 units distributed worldwide.
Integra LifeSciences is recalling 915 units of its Cranial Access Kit worldwide due to defective sterile packaging that may compromise product sterility. The header bags failed required packaging integrity testing.
The NxStage Cartridge Express dialysis device is recalled because blood can leak or spray from the arterial line. This could cause uncontrolled blood loss in patients or expose healthcare workers to infectious blood.
Ancient Formulas' Healthprint Vitamin D3 5000 supplement contains less Vitamin D than claimed and has incorrect daily value labeling. The recall affects 111 bottles distributed in Florida.
Abbott Molecular recalls five Vysis in-vitro diagnostic kits that were intended for export and shipped to U.S. customers without approval or registration per U.S. specifications.
Seatex LLC is recalling 1,450 cases of PROBLEND Antibacterial Foaming Hand Sanitizer due to Current Good Manufacturing Practice (CGMP) deviations discovered at its manufacturing facility. The recall affects product distributed nationwide in the United States and Puerto Rico.
A hand sanitizer distributed to 7-Eleven gas stations nationwide is being recalled due to manufacturing deficiencies identified during an FDA inspection. The affected product is lot 251176, distributed in the United States and Puerto Rico.
Seatex LLC is recalling PROBLEND E3 Foaming Hand Sanitizer due to manufacturing practice deviations identified during FDA inspection. The recall affects products distributed nationwide in the US and Puerto Rico.
Seatex LLC is recalling PROBLEND Hand Sanitizer (Lot 266029) nationwide due to manufacturing deficiencies identified during FDA inspection.
GRAPHENANO Dental G-CAM denture manufacturing material is being recalled due to machining errors that render the product unusable. The recall affects 354 units distributed in Utah.
EMD Millipore has recalled Schiff Reagent Hotchkiss-McManus (lots 3094 and 3096) because units appear pink instead of colorless. Laboratories should discontinue use of affected units distributed to US states and Canada.
Abbott Molecular recalled M1000 Wash Station units shipped to U.S. customers without FDA approval or registration. The devices were intended for export only and not approved for U.S. distribution.
Abbott Molecular shipped two in-vitro diagnostic FISH probe kits to U.S. customers that were intended for export only and not approved or registered per U.S. specifications. The recall affects 16 kits distributed across eight states.
Parker Laboratories is recalling Tensive Conductive Adhesive Gel due to five complaints regarding incorrect viscosity. The affected product was distributed across multiple US states and internationally.
Lippert is recalling Utility Hub Oil Seals that may leak oil onto brake components, potentially reducing braking ability and increasing crash risk.
Nissan North America is recalling certain 2024 Nissan Pathfinder and Infiniti QX60 vehicles. The left-side front lap seat belt pretensioner may be improperly secured due to a missing rivet, which could prevent proper occupant restraint during a crash.
The tire placard label on certain 2023-2024 Alfa Romeo Tonale and Dodge Hornet vehicles displays an incorrect maximum vehicle capacity weight value, which could lead to vehicle overloading and increased crash risk. Dealers will add an overlay label to correct the information.
Certain 2022-2023 NOVA BUS LFS vehicles may have missing electrical components that prevent the battery disconnect switch from functioning properly, creating a risk of electrical shock during maintenance.
CJ Foods Manufacturing Beaumont Corporation is recalling Trader Joe’s Steamed Chicken Soup Dumplings due to possible contamination with hard plastic from a permanent marker pen.
Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because the main wiring harness may chafe and short circuit, increasing the risk of fire and loss of vehicle control.
Mercedes-Benz is recalling 2022-2023 G 550 and AMG G 63 vehicles because the air-conditioning system may contain incorrect refrigerant, which could leak and increase fire risk in a crash.
Mack Trucks is recalling 2024 MD6 and MD7 vehicles because the park brake light may display the wrong status, potentially allowing the vehicle to roll away.
Faraday Future is recalling 2023 FF-91 Alliance vehicles because a software error may prevent the air bag malfunction warning light from illuminating, increasing crash injury risk.
Kia is recalling 2018-2023 Stinger and 2019-2020 K900 vehicles due to potential engine fire from deteriorating turbocharger oil feed pipes.
Mack Trucks is recalling 2024 Granite vehicles because incorrect Gross Axle Weight Rating labels may allow the vehicles to be overloaded, increasing crash risk.
Winnebago is recalling 2023-2024 Sunstar motorhomes because the tire information label incorrectly states the tire size and Gross Vehicle Weight Rating.
Winnebago is recalling 2024 Solis motorhomes because the lavatory may have a standard outlet instead of a GFCI protected one, increasing the risk of electric shock.
Looking for a different month? Back to 2024.