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
Freshire Farms jalapenos packaged in 8-ounce bags are being recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,298 cases distributed across nine states.
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.
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.
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.
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 Poblano peppers in multiple package formats due to potential Listeria monocytogenes contamination. The affected product was distributed across nine U.S. states.
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.
Metro Produce Distributors is recalling Lunds & Byerlys Smokin' Guacamole Dip due to possible Listeria monocytogenes contamination. The 10 oz product was distributed in Minnesota.
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.
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.
Foppen Smoked Norwegian Salmon Slices (8.1oz vacuum foil packages) are recalled due to potential contamination with Listeria monocytogenes. The recall affects 747 cases distributed across 15 U.S. states.
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.
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.
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.
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.
RS Hanline and Company Inc is recalling green peppers due to potential Listeria monocytogenes contamination. The recall affects peppers distributed across nine states.
Lunds & Byerlys Deli Guacamole (Item 85999, 56 oz) may be contaminated with Listeria monocytogenes. Twenty-eight units with a Use By date of 02-AUG-24 were distributed in Minnesota.
Becton Dickinson & Co. is recalling the BD Kiestra Urine Culture Application due to a software issue that may cause inaccurate bacterial colony counts. This could impact patient diagnosis and treatment decisions.
Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage that may pose patient safety risks in cardiac and vascular procedures.
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.
Pariva LLC is recalling Pariva Marinated Labneh Bites Mild Tandoori due to potential mold contamination. Affected products were distributed in Massachusetts, Maine, New Hampshire, Rhode Island, New York, New Jersey, and Connecticut.
Merit Medical convenience kits containing plastic syringes have been recalled nationwide. The syringes have quality issues including leaks and breakage that may pose a risk to patient health.
Beckman Coulter has recalled 183 DxI 9000 Access analyzers due to a software issue that causes delays in test result reporting. When connected to a Laboratory Automation System, software versions 1.17 and below send out-of-sequence messages, potentially delaying patient treatment.
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 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.