The Recall Desk

Recalls

All US Product 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.

How to read this listing

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.

Filters

Agency

Category

Minimum severity

Clear filters

1576–1600 of 36519

  • CriticalFDA (Devices)·Z-0057-2026·2025-10-22

    BF-P190 bronchovideoscopes recalled for clarified laser and coagulation instructions

    Olympus is recalling EVIS EXERA III Bronchovideoscope BF-P190 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0095-2026·2025-10-22

    Pacemakers recalled for software update preventing Safety Mode from battery impedance

    Boston Scientific is recalling 223,163 ESSENTIO DR SL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    Model Number L111, ESSENTIO DR SL MRI Pacemaker
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0081-2026·2025-10-22

    ACCOLADE single chamber pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 50,135 ACCOLADE SR SL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    ACCOLADE SR SL MRI (Model L310)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0067-2026·2025-10-22

    Cantaloupe honeydew grape mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling cut fresh fruit mix of cantaloupe, honeydew and red grapes under several brands for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix "HC" 6/6oz. UPC 7 90629-11821 6. 2. Fruit Medley "F&F" 4/12 oz. Fresh & Finest UPC 0 70253-00573 2 3. Fruit Mix 4/16 oz,
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0062-2026·2025-10-22

    Cut fresh fruit salad recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling Harvest Cuts Cut Fresh Fruit Salad for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Salad. 6/6 oz. Harvest Cuts. Contains: Cantaloupe, Honeydew, Red Grape, Strawberry. Keep Refrigerated. Packed in the following container sizes: 1. 6/6 oz. UPC 7 90629-11822 3. 2. 4/16 oz. UPC 7 90629-08009 4. Packed by WPS, Minneapolois, MN
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0084-2026·2025-10-22

    ACCOLADE dual chamber extended life MRI pacemakers recalled for software update

    Boston Scientific is recalling 34,180 ACCOLADE DR EL MRI pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    ACCOLADE DR EL MRI (Model L331)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0089-2026·2025-10-22

    PROPONENT dual chamber pacemakers recalled for Safety Mode software update

    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.

    Product
    Model Number L211 PROPONENT DR SL MRI Pacemaker
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0055-2026·2025-10-22

    Large white eggs in cartons recalled over 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.

    Product
    Free Range Grade AA Large White Eggs, 12ct Cartons, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·H-0048-2026·2025-10-22

    Free range brown eggs recalled over 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.

    Product
    Free Range Grade A Large Brown Eggs, 18ct Cartons, UPC: 860010568538, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-0051-2026·2025-10-22

    BF-1TQ180 bronchovideoscopes recalled for updated therapy equipment use instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type 1TQ180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0062-2026·2025-10-22

    BF-Q180-AC bronchovideoscopes recalled for updated laser and coagulation use instructions

    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.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0096-2026·2025-10-22

    ESSENTIO dual chamber extended life pacemakers recalled for software update

    Boston Scientific is recalling 10,833 ESSENTIO DR EL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    Model Number L121 ESSENTIO DR EL Pacemaker
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0072-2026·2025-10-22

    Plain cheesecakes recalled because the product contains undeclared pecan

    Eli's Cheesecake Company is recalling 2,216 Wegmans Ultimate Plain Cheesecakes because the product contains undeclared pecan.

    Product
    Wegmans Ultimate Plain Cheesecake Large Net Wt 3.13 lb (1.42kg), shrink wrapped in a collar, 8 cakes per wholesale case
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Devices)·Z-0058-2026·2025-10-22

    BF-P60 bronchofiberscopes recalled for updated instructions on laser and coagulation use

    Olympus is recalling OES Bronchofiberscope BF Type P60 units for additional instructions-for-use updates clarifying safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0102-2026·2025-10-22

    VALITUDE MRI resynchronization pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 28,911 VALITUDE CRT-P EL MRI devices, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    Model Number U128, VALITUDE CRT-P EL MRI
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0101-2026·2025-10-22

    VALITUDE resynchronization pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 3,620 VALITUDE CRT-P EL devices, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    Model Number U125, VALITUDE CRT-P EL
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0087-2026·2025-10-22

    PROPONENT VDD pacemakers recalled for Safety Mode software architecture update

    Boston Scientific is recalling 3,146 PROPONENT DR (VDD) SL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    Model Number L209 PROPONENT DR (VDD) SL Pacemaker
    Category
    Medical Device
    Distribution
    0 states