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
ICU Medical is recalling 130,826 units of Plum 360/A+ spare batteries due to a manufacturing defect that causes earlier-than-expected battery capacity loss and reduced runtime.
ICU Medical is recalling Plum A+ and Plum A+3 infusion pump batteries due to a manufacturing defect that may cause premature capacity loss and reduced runtime. Approximately 14,744 units were distributed worldwide.
RS Hanline and Company Inc is recalling Poblano peppers in multiple package formats due to potential Listeria monocytogenes contamination. The affected product was distributed across nine U.S. states.
Publix Super Markets is recalling 2,786 units of Boars Head Grab and Go Wedge Ham products due to potential Listeria monocytogenes contamination. The affected products were sold at retail locations in Florida and Georgia.
Metro Produce Distributors is recalling Lunds & Byerlys Fresh Guacamole Dip due to potential Listeria monocytogenes contamination. The affected product has a Use By date of 02-AUG-24 and was distributed in Minnesota.
Defibtech is recalling the RMU-2000 Automated Chest Compression Device because a motor defect may cause the device to stop delivering compressions, potentially delaying critical therapy and resulting in patient injury or death.
North Fish USA is recalling Cold Smoked Capelin packages due to potential Clostridium botulinum contamination in uneviscerated fish. The affected products were distributed in Georgia and New York.
Van Leeuwen Ice Cream is recalling Pumpkin Cinnamon Roll non-dairy frozen dessert (14 oz) due to undeclared peanuts. The allergen poses serious risk to consumers with peanut allergies.
Metro Produce Distributors is recalling 121 units of Lunds & Byerlys Spicy Guacamole Dip because it may be contaminated with Listeria monocytogenes. The affected product was distributed in Minnesota.
RS Hanline and Company Inc is recalling Freshire Farms Green Beans due to potential Listeria monocytogenes contamination. Approximately 1150 cases were distributed across nine states.
RS Hanline and Company Inc is recalling green peppers due to potential Listeria monocytogenes contamination. The recall affects peppers distributed across nine states.
Metro Produce Distributors is recalling Lunds & Byerlys Smokin' Guacamole Dip due to possible Listeria monocytogenes contamination. The 10 oz product was distributed in Minnesota.
Metro Produce Distributors is recalling 66 units of Lunds & Byerlys Pico de Gallo/Guacamole Dip distributed in Minnesota due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
ICU Medical is recalling Plum 360 Infusion System replacement batteries due to a manufacturing defect that may cause loss of capacity and decreased runtime earlier than expected. Approximately 11,961 units were distributed worldwide.
Merit Medical convenience kits used in cardiac procedures contain plastic syringes with potential leaks and breakage. The defects were identified following an FDA Safety Alert issued March 19, 2024.
Thoratec LLC is recalling 694 HeartMate 3 System Controllers because the UI membrane may lift along the housing, allowing fluid entry that could damage internal circuits and cause loss of power or pump failure.
FDC Limited recalls Timolol Maleate eye drops (362,544 bottles) nationwide due to a manufacturing defect: a yellow spike from the cap lodged in the nozzle, posing a risk of eye injury.
Palodex Group Oy recalls the Orthopantomograph OP300 dental x-ray system due to a testing software defect that may allow devices with poor image repeatability to be distributed.
Merit Medical convenience kits containing recalled plastic syringes have quality issues including leaks and breakage that may pose risks during vascular and cardiac procedures. Approximately 5,700 affected kits were distributed nationwide.
Merit Medical is recalling paracentesis procedure kits nationwide containing syringes with identified leaks and breakage. The defects may pose a risk to patient health during medical procedures.
Aurora Series surgical light heads are recalled due to cracked welds on the frame. The defects can cause the frame to sag, housing to crack, or the light head to detach.
EYE COMFORT CARE LLC is recalling the UNclog Eye Mask due to safety clips that may allow wires to detach, potentially causing electrical shorts and burn injuries.
Pariva LLC is recalling Pariva Marinated Labneh Bites Za'atar (8 oz) due to potential mold contamination. The product was distributed in seven Northeast states with best-by dates in October or December 2024.
Merit Medical is recalling 3,631 catheter extractor convenience kits due to defective syringes with leaks and breakage. The identified quality issues may compromise patient safety during catheter removal.
Merit Medical is recalling medical convenience kits with defective syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health during procedures.