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.

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4801–4825 of 89480

  • 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-0110-2026·2025-10-22

    Curve D-D ablation catheters recalled after tip detachment from packaging

    Abbott is recalling 3,404 TactiFlex Sensor Enabled Ablation Catheters in the D-D curve after becoming aware of tip detachment events during removal from the packaging.

    Product
    TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DD, (BiD Curve D-D), REF A-TFSE-DD; cardiac catheter
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0113-2026·2025-10-22

    UniD curve F ablation catheters recalled after tip detachment from packaging

    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.

    Product
    TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, F, (UniD Curve F), REF A-TFSE-F; cardiac catheter
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0064-2026·2025-10-22

    Cut fruit with dip recalled over potential Listeria monocytogenes contamination

    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.

    Product
    Cut Fresh Fruit with Fruit Dip. 2 lbs. Contains: Cantaloupe, Honeydew, Pineapple, Red Grapes, & Fruit Dip. Keep Refrigerated. Packed under the following brands: 1. Fresh & Finest. UPC 0 70253-00615 9 2. Harvest Cuts. UPC 0 7 90629-13772 9. Packed by WPS, Minneapol
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0063-2026·2025-10-22

    Cut fruit mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling 307 cases and pails of Fresh & Finest Cut Fresh Luau Blend Fruit Mix for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Luau Blend Fruit Mix "F&F". 4/10 oz. Fresh & Finest. Contains: Cantaloupe, Honeydew, Pineapple, Red Grapes, Strawberry, Blueberry. Keep Refrigerated. UPC 0 70253-00572 5. Packed by WPS, Minneapolois, MN
    Category
    Food
    Distribution
    5 states
  • 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-0067-2026·2025-10-22

    BF-XT40 bronchofiberscopes recalled for updated therapy equipment use instructions

    Olympus is recalling OES Bronchofiberscope BF Type XT40 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (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-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 (Devices)·Z-0085-2026·2025-10-22

    PROPONENT single chamber standard life pacemakers recalled for software update

    Boston Scientific is recalling 1,380 PROPONENT SR SL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    PROPONENT SR SL (Model L200)
    Category
    Medical Device
    Distribution
    0 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 (Food)·H-0059-2026·2025-10-22

    Cut cantaloupe chunks recalled over potential Listeria monocytogenes contamination

    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.

    Product
    Cut Fresh Cantaloupe Chunks packaged into the following size containers some under brand names Fresh & Finest or Harvest Cuts: 1. CANTALOUPE CHUNKS "PRMK" 30/2 OZ 2. CANTALOUPE CHUNKS "HC" 6/6 OZ. Harvest Cuts UPC 7 90629-11820 9. 3. CANTALOUPE CHUNKS "HC" 24/8 OZ.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0053-2026·2025-10-22

    Loose large white eggs recalled over potential Salmonella contamination on pallets

    Black Sheep Egg Company is recalling 7,200 dozen Free Range Grade AA Large White Eggs sold loose on open skids for potential Salmonella contamination.

    Product
    Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-0105-2026·2025-10-22

    VISIONIST MRI resynchronization pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 41,191 VISIONIST 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 U228, VISIONIST CRT-P EL MRI
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0082-2026·2025-10-22

    ACCOLADE dual chamber MRI pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 90,931 ACCOLADE 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
    ACCOLADE DR SL MRI (Model L311)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0100-2026·2025-10-22

    ALTRUA 2 dual chamber extended life pacemakers recalled for software update

    Boston Scientific is recalling 3,376 ALTRUA 2 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 S722, ALTRUA 2 DR EL Pacemaker
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0083-2026·2025-10-22

    ACCOLADE dual chamber extended life pacemakers recalled for software update

    Boston Scientific is recalling 7,488 ACCOLADE DR EL 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 (Model L321)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0080-2026·2025-10-22

    ACCOLADE dual chamber standard life pacemakers recalled for software update

    Boston Scientific is recalling 32,695 ACCOLADE DR SL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    ACCOLADE DR SL (Model L301)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0066-2026·2025-10-22

    Melon and grape mix recalled over potential Listeria monocytogenes contamination

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

    Product
    Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Watermelon and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHWG (MCT) 1/5 lb. UPC 7 90629-11173 6. 2. Melon Mix Bowl & Grapes "HC" 2/48 oz. Harvest Cuts UPC 7 90629-10225
    Category
    Food
    Distribution
    5 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