Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
The MAGEC 1 System implantable medical device is being recalled due to documented post-implantation fractures of an internal metallic component. The recall affects approximately 3,056 units manufactured before March 26, 2015 and distributed worldwide.
G&C Food Distributors & Brokers Inc. is recalling Gouda cheese that may contain undeclared wheat. The product was distributed to food service facilities in Connecticut, New Jersey, New York, Pennsylvania, and Tennessee.
Velano Vascular is recalling 123,700 PIVO Blood Collection Device 20G units due to incomplete package sealing that could compromise sterile barriers and allow microbial contamination.
Edge Pharma is recalling Ceftazidime sterile ophthalmic solution for intraocular injection due to lack of assurance of sterility. The recall affects 168 syringes distributed nationwide.
BAOPTEIL-branded children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. About 3,800 units sold from December 2019 through August 2021 are affected.
Edge Pharma, LLC is recalling Methacholine Challenge 5-Syringe Test Kits nationwide due to lack of assurance of sterility. The sterile inhalation solution may not meet sterility standards.
Porsche is recalling one 2021 Taycan with misaligned front and rear suspension. The misalignment may cause uneven tire wear and increase crash risk.
Siemens is recalling 23 Artis icono angiography systems due to four software defects that could disable imaging, corrupt images, and cause unexpected shutdowns during patient procedures.
Siemens is recalling its Artis pheno diagnostic angiography system (12 units) due to four software defects that may prevent imaging, corrupt images, or cause unintended shutdowns during clinical use.
Tiffin is recalling 2020-2022 Allegro Red motorhomes because the patio awning may have been improperly installed and could detach while driving, increasing crash and injury risk.
Siemens is recalling 72 units of Artis icono biplane diagnostic imaging systems nationwide due to four software issues that could disable x-ray capability, corrupt diagnostic images, or cause unexpected shutdowns during procedures.
FDA recalls Intelli-C footrest accessories due to missing friction rubber blocks in the clamping mechanism. The defect may cause the footrest to slip during use.
Beaverton Foods Inc is recalling Inglehoffer Seafood Tartar Sauce with Lemon & Capers because the ingredient label declares soybean oil but does not adequately disclose soy as an allergen, posing a risk to consumers with soy allergies.
Keystone is recalling 2021-2022 Raptor and 2021 Montana RVs with certain Sailun tires that may experience belt separation. Belt separation could cause loss of vehicle control and increase crash risk.
World Health Products LLC is recalling GAT SPORT JETFUEL DIURETIC capsules because they may contain undeclared milk, a common allergen. The product was distributed across most U.S. states and internationally.
Edge Pharma is recalling approximately 5,335 syringes of Phenylephrine HCl Sterile Solution for Injection nationwide due to lack of assurance of sterility. The product may not meet sterility requirements for safe use.
Edge Pharma is recalling a sterile ophthalmic solution (Phenylephrine HCl/Tropicamide 2.5%/1%) because the manufacturer cannot assure sterility of the product. The recall affects 363 droptainers distributed nationwide.
Tesla is recalling 2020-2022 Model Y, S, X, and 3 vehicles due to a heat pump software error that reduces windshield defrosting performance. This may decrease driver visibility and increase crash risk.
Relish Foods, Inc. dba Gourmet Fusion Foods is recalling 10 oz. individually wrapped frozen tuna steaks due to elevated histamine levels detected in FDA consumer samples.
Bake Crafters is recalling Maple Waffle WG Chicken Sausage due to potential Listeria monocytogenes contamination. The affected products were distributed to distribution centers in Idaho and Pennsylvania.
Brownie Points LLC is recalling Brownie Points Schmurtle brownies because the label does not disclose peanuts as an allergen. The product was distributed across the United States in gift baskets.
Games Workshop is recalling about 2,600 KOYO Bounca The Squig Limited Edition Plush toys because the pom-poms can detach, posing a choking hazard to young children. No injuries have been reported.
Edge Pharma, LLC is recalling Methotrexate, USP, Sterile Solution for Injection (125 mg/5mL) due to lack of assurance of sterility. The recall affects 457 syringes distributed nationwide.
G&C Food Distributors & Brokers Inc. is recalling white cheddar cheese distributed to Connecticut, New Jersey, New York, Pennsylvania, and Tennessee because the product may contain undeclared wheat, which poses a risk to consumers with wheat allergies.
Biomerieux is recalling API ID 32 C Strips due to a thermoforming defect that risks misidentification of yeasts or delayed diagnostic results. The recall affects 462 kits in Arizona, Iowa, Kentucky, and New York.