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
Boston Scientific is recalling 106,536 PROPONENT DR SL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.
Abbott is recalling 1,960 TactiFlex Sensor Enabled Ablation Catheters in the UniD curve F configuration after becoming aware of tip detachment events during removal from the packaging.
Boston Scientific is recalling 63,851 PROPONENT DR EL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.
Boston Scientific is recalling 190,088 ESSENTIO DR EL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.
Wholesale Produce Supply is recalling 2 lb Cut Fresh Fruit with Fruit Dip trays under the Fresh & Finest and Harvest Cuts brands for potential Listeria monocytogenes contamination.
Black Sheep Egg Company is recalling 23,625 dozen Free Range Grade A Large Brown Eggs in 12-count cartons for potential Salmonella contamination.
Black Sheep Egg Company is recalling 16,245 dozen Free Range Grade A Large Brown Eggs in 18-count cartons for potential Salmonella contamination.
Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Medium White Eggs in 18-count cartons for potential Salmonella contamination.
Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Large White Eggs in 12-count cartons for potential Salmonella contamination.
Black Sheep Egg Company is recalling 288,900 dozen Free Range Grade AA Large Brown Eggs sold loose on open skids for potential Salmonella contamination.
Boston Scientific is recalling 3,592 PROPONENT DR EL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.
Wholesale Produce Supply is recalling 12 oz Fresh & Finest Cut Fresh Cantaloupe & Honeydew Chunks for potential Listeria monocytogenes contamination.
Wholesale Produce Supply is recalling Harvest Cuts Cut Fresh Fruit Salad for potential Listeria monocytogenes contamination.
Olympus is recalling Bronchovideoscope BF-Q170 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Wholesale Produce Supply is recalling cut fresh fruit mix under several brands and sizes for potential Listeria monocytogenes contamination.
D & M Smoked Fish is recalling 2,022 pieces of Haifa Cold Smoked Salmon because the product is contaminated with Listeria monocytogenes.
Wholesale Produce Supply is recalling Cut Fresh Cantaloupe Chunks in several container sizes under the Fresh & Finest and Harvest Cuts brands for potential Listeria monocytogenes contamination.
Black Sheep Egg Company is recalling 46,800 dozen Free Range Grade AA Medium White Eggs sold loose on open skids for potential Salmonella contamination.
Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type Q180-AC units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Black Sheep Egg Company is recalling 20,625 dozen Free Range Grade AA Large Brown Eggs loose packed in boxes for potential Salmonella contamination.
Olympus is recalling OES Bronchofiberscope BF Type 1T60 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling OES Bronchofiberscope BF Type MP60 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling Bronchovideoscope BF-1TQ170 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling Bronchovideoscope BF-H1100 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling Bronchovideoscope BF Type 1T150 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.