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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6326–6350 of 113876

  • 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-0047-2026·2025-10-22

    Large brown eggs recalled over potential Salmonella contamination in twelve count cartons

    Black Sheep Egg Company is recalling 23,625 dozen Free Range Grade A Large Brown Eggs in 12-count cartons for potential Salmonella contamination.

    Product
    Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-0097-2026·2025-10-22

    ESSENTIO extended life MRI pacemakers recalled for Safety Mode software update

    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.

    Product
    Model Number L131, ESSENTIO DR EL MRI Pacemaker
    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 (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-0091-2026·2025-10-22

    PROPONENT dual chamber extended life MRI pacemakers recalled for software update

    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.

    Product
    Model Number L231, PROPONENT DR EL MRI Pacemaker
    Category
    Medical Device
    Distribution
    0 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
  • 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-0053-2026·2025-10-22

    BF-H190 bronchovideoscopes recalled for updated laser and coagulation use instructions

    Olympus is recalling EVIS EXERA III Bronchovideoscope BF-H190 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-H190
    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 (Drugs)·D-0015-2026·2025-10-22

    Compounded oxytocin bags recalled after testing found no oxytocin present

    IntegraDose Compounding Services is recalling 853 bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride after testing revealed there was no oxytocin in the IV bag.

    Product
    Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0065-2026·2025-10-22

    Cut melon mix recalled over potential Listeria monocytogenes contamination

    Wholesale Produce Supply is recalling cut fresh melon mix under several brands and sizes for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Melon Mix. Contains: Cantaloupe, Honeydew, Watermelon. Keep Refrigerated. Packed under the following brands and sizes: 1. Melon Mix "HC" 4/16 oz. Harvest Cuts UPC 7 90629-11844 5. 2. Melon Mix CHW (MCT) 1/5 lb. UPC 7 90629-11173 6. 3. Melon Mix Bowl "HC"
    Category
    Food
    Distribution
    5 states
  • 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-0090-2026·2025-10-22

    PROPONENT pacemakers recalled for Safety Mode software architecture update

    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.

    Product
    Model Number L221 PROPONENT DR EL Pacemaker
    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 (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-0112-2026·2025-10-22

    Curve F-J ablation catheters recalled after tip detachment during unpacking

    Abbott is recalling 11,810 TactiFlex Sensor Enabled Ablation Catheters in the F-J curve after becoming aware of tip detachment events during removal from the packaging.

    Product
    TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, FJ, (BiD Curve F-J), REF A-TFSE-FJ; cardiac catheter
    Category
    Medical Device
    Distribution
    0 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-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