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
Renaissance Food Group is recalling Spicy Guacamole Blender products because positive test results confirmed Listeria monocytogenes contamination in the finished product.
Renaissance Food Group is recalling Hatch Chile Guacamole Blender due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Diced Red Onion (10 oz units) distributed to Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in finished product.
Renaissance Food Group is recalling diced bell pepper and white onion products due to positive test results for L. monocytogenes. The recalled products were distributed in Alabama, Georgia, and South Carolina.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
Eden's Answers Inc is recalling Sprigs Lil Ones Sleepy Time herbal supplement due to high bacterial growth in the product. Consumers should stop using it immediately.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Pfizer is recalling Aminophylline Injection vials due to a complaint of particulate matter (hair) in one vial. Over 103,000 vials were distributed to the US and Puerto Rico.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
B. Braun is recalling 94,000 Introcan Safety FEP 14G catheters due to potential leakage at the catheter hub. Affected units were distributed in the US and Canada.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Salon Technologies International is recalling Sanitizing Hand Spray 80% due to GMP deviations: the product contains acetaldehyde and acetal above specification limits. The recall affects 1,656 bottles distributed in Florida and Washington.
Aurora Products is recalling its Aurora Natural brand Organic Cranberry Frontier Mix due to undeclared peanuts. People with peanut allergies are at risk.
Coca-Cola Southwest Beverages LLC is recalling Coca-Cola Classic 12 FL OZ metal cans in 12-pack fridge packs due to the presence of metal particles in the product.
FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.
Kia is recalling certain 2021-2023 K5 and 2021-2022 Sorento vehicles with transmission oil pump malfunction that may cause complete loss of drive power, increasing crash risk.
Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.
Chrysler is recalling specific Mopar brake hoses because the inside diameter may be too small, causing rupture and loss of braking ability.
Wabash National is recalling 2020-2023 RFALHSA trailers because the lift gate obscures rear conspicuity tape, reducing visibility and increasing crash risk.