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 deaths or serious injuries are reported, 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
Olympus Corporation of the Americas is recalling 3,354 units of the OER-Pro endoscope reprocessor because MAJ-1443 and MAJ-1444 accessories are no longer compatible with it.
Olympus is recalling 444 units of the PK Cutting Forceps (Model PK-CF0533) worldwide because defective welds in supplier-provided components can cause the instrument's jaw to break during surgical use.
Medtronic MiniMed 780G insulin pumps with software versions 6.60, 6.61, and 6.62 may have three software defects causing inaccurate insulin delivery, risking hypoglycemia or hyperglycemia.
Tandem insulin pumps in Czech Republic and Slovakia are recalled for translation errors. An error tells users to verify infusion set connection when it should state not connected, risking unintended insulin delivery and hypoglycemia.
Olympus Endoscope Reprocessor OER-Elite is no longer compatible with MAJ-1443 and MAJ-1444 endoscope models. Affected endoscopes may not be properly sterilized when processed in this reprocessor, creating infection risk.
I.T.S. LRS surgical implants are recalled because updated MRI testing shows higher temperature increases than documented in labeling. 176 units affected nationwide.
Olympus recalled 106 Everest Bipolar Cutting Forceps (Model 3005) due to defective welds in supplier-provided components. The defect can cause the forceps' jaw to break during surgery.
TECNIS Eyhance intraocular lenses are being recalled because a haptic may stick to the optic, preventing proper unfolding during implantation. A limited quantity of 361 units was distributed nationwide.
I.T.S. surgical plates and screws are recalled because updated testing found higher radiofrequency-induced heating during MRI than stated in original instructions.
Straumann USA recalled 7 Custom Abutment AS Ti units due to a manufacturing error in which a TAN material bar was incorrectly used instead of titanium.
Tops GOLD Green Chilli Pickle, 31.74 oz cans, is recalled due to potential adulteration with erucic acid from mustard oil. The product was distributed in CA, NV, OR, UT, and WA.
I.T.S. GmbH is recalling Pilonplate with Angular Stability orthopedic surgical plates due to MRI safety concerns. Updated testing shows higher radiofrequency-induced temperature increases during MRI than previously documented in the product's instructions.
Pacific Coast Fresh CO is recalling King Harvest brand Spinach Hummus (10 oz containers) due to the presence of aluminum pieces in the product. Consumers should not consume the product and should return or discard it.
Nuts.com is recalling Espresso Malted Milk Balls sold in 1 lb. and 20 lb. packages because the labels do not declare wheat and soy allergens that are present in the product.
Distribuidora de Alimentos Sendero LLC is recalling Doraditas de Azucar because the product label is missing declarations for wheat and soy allergens.
Ajinomoto Foods North America Inc. is recalling Ajinomoto Green Gyoza Vegetable & Edamame Dumplings due to the presence of glass fragments (1–3 cm long and 2–4 mm wide) in the product.
Ajinomoto Foods North America is recalling Item 81097 Ling Ling Restaurant Style Fried Rice due to glass fragments measuring 1-3 cm long and 2-4 mm wide found in the product. Affected units with Best By dates 9/21/2026 through 3/8/2027 were distributed across 40 U.S. states.
Rose and Shore, Inc. is recalling 14" Margarita Thin Crust Pizza due to potential metal pieces found in the tomato ingredient. The product was distributed to retail locations in California, Oregon, Arizona, Idaho, and Texas.
Ajinomoto Foods North America Inc. is recalling Vegetable Gyoza Dumplings (UPC 071757055483) due to the presence of glass fragments in the product, which could pose a choking or injury hazard if ingested.
Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.
Lidl US is recalling Favorina Chocolate Ladybugs German-Style Nougat because the label does not specify which tree nut is contained in the product, posing a risk to consumers with tree nut allergies.
King Harvest brand Roasted Red Pepper Hummus is being recalled due to the presence of aluminum pieces in the product. The affected hummus was distributed in Oregon and Washington.
I.T.S. GmbH is recalling Pelvic Reconstruction System implants because updated MRI safety testing revealed higher radiofrequency-induced temperatures than originally documented. This discrepancy between the devices' actual heat generation and the instructions could pose a burn risk during MRI procedures.
Medline Industries is recalling Puracol and Puracol Plus Collagen Wound Dressings due to elevated endotoxin levels. Affected products may cause tissue irritation, delayed healing, or in severe cases, septic shock.
PACCAR is recalling certain 2023-2024 Peterbilt and Kenworth trucks whose throttle pedal assemblies may contain an oversized magnet carrier, causing the pedal to stick or respond slowly. A sticking pedal increases crash risk.