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 the agency’s own highest classification or reported deaths or serious injuries, 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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1976–2000 of 39704

  • CriticalFDA (Devices)·Z-0031-2026·2025-10-22

    Percussive ventilation valves recalled over leak risk in small patients

    Percussionaire is recalling 59,160 Phasitron 5 IPV in-line valves whose pressure relief seal may leak when used with a ventilator, and is warning against use in neonates and infants.

    Product
    Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0086-2026·2025-10-22

    PROPONENT dual chamber standard life pacemakers recalled for software update

    Boston Scientific is recalling 2,426 PROPONENT DR SL pacemakers, part of a software update designed to prevent Safety Mode starting outside hospital because of a high battery impedance state.

    Product
    PROPONENT DR SL (Model L201)
    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 (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-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…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0060-2026·2025-10-22

    Cantaloupe and honeydew chunks recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling 12 oz Fresh & Finest Cut Fresh Cantaloupe & Honeydew Chunks for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Cantaloupe & Honeydew Chunks Fresh & Finest. Net Wt: 12 oz Keep Refrigerated. UPC 0 70253-00582 4. Packed by WPS, Minneapolois, MN
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0043-2026·2025-10-22

    Thoracic endovascular grafts recalled over coating scrapings that may embolize

    Cook Medical is recalling 695 Zenith Alpha 2 Thoracic Endovascular Grafts because affected devices may contain PTFE coating scrapings that could be released during deployment.

    Product
    Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167 ZTA2-P-40-167-W ZTA2-P-40-217-W ZTA2-P-42-121 ZTA2-P-42-121-W ZTA2-P-42-173 ZTA2-P-42-173-W ZTA2-P-42-225 ZTA2-P-42-225-W ZTA2-P-44-125…
    Category
    Medical Device
    Distribution
    31 states
  • CriticalFDA (Food)·H-0069-2026·2025-10-22

    Fruit trays with watermelon recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling Harvest Cuts Fruit Trays with Watermelons for potential Listeria monocytogenes contamination.

    Product
    Harvest Cuts Fruit Tray with Watermelons. Contains: Cantaloupe, Honeydew, Pineapple, Watermelon, Red Grapes, Fruit Dip. Keep Refrigerated. Net Wt. 2 lbs. 8 oz. UPC 7 90629-07997 5. Packed by WPS, Minneapolois, MN
    Category
    Food
    Distribution
    5 states
  • 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-0063-2026·2025-10-22

    BF-Q190 bronchovideoscopes recalled for clarified laser and coagulation instructions

    Olympus is recalling EVIS EXERA III Bronchovideoscope BF-Q190 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-Q190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0054-2026·2025-10-22

    Medium white eggs recalled over potential Salmonella contamination across many lots

    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.

    Product
    Free Range Grade AA Medium 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-0098-2026·2025-10-22

    ALTRUA 2 single chamber pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 4,841 ALTRUA 2 SR 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 S701 ALTRUA 2 SR SL Pacemaker
    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 (Devices)·Z-0088-2026·2025-10-22

    PROPONENT single chamber pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 41,009 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
    Model Number L210 PROPONENT SR SL Pacemaker
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0061-2026·2025-10-22

    BF-Q180 bronchovideoscopes recalled for updated laser and coagulation instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type Q180 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
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0056-2026·2025-10-22

    Medium white eggs in cartons recalled over 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.

    Product
    Free Range Grade AA Medium White Eggs, 18ct Cartons, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
    Category
    Food
    Distribution
    6 states