The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

426–450 of 7436

  • 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-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 (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-0094-2026·2025-10-22

    ESSENTIO single chamber MRI pacemakers recalled for Safety Mode software update

    Boston Scientific is recalling 61,700 ESSENTIO 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
    Model Number L110, ESSENTIO SR SL MRI Pacemaker
    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-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-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-0061-2026·2025-10-22

    Cut fruit trays with strawberries recalled over potential Listeria contamination

    Wholesale Produce Supply is recalling Harvest Cuts 2.5 lb Cut Fresh Fruit Trays with Strawberries for potential Listeria monocytogenes contamination.

    Product
    Cut Fresh Fruit Tray with Strawberries. 2.5 LB Harvest Cuts. Keep Refrigerated. UPC 7 90629-08132 9. 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-0109-2026·2025-10-22

    UniD curve ablation catheters recalled after tip detachment from packaging

    Abbott is recalling 407 TactiFlex Sensor Enabled Ablation Catheters in the UniD curve D configuration after becoming aware of tip detachment events during removal from the packaging.

    Product
    TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, D, (UniD Curve D), REF A-TFSE-D; 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 (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-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 (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-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 ZTA2-P-44-1
    Category
    Medical Device
    Distribution
    31 states
  • CriticalFDA (Food)·H-0068-2026·2025-10-22

    Cut fresh fruit mix recalled over potential Listeria monocytogenes contamination

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

    Product
    Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHPG (MCT) 1/5 lb. 2. Fruit Medley "HC" 24/8 oz. Harvest Cuts UPC 7 90629-08008 7. 3. Fruit Mix CHPG (PAIL)
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0046-2026·2025-10-22

    BF-1T180 bronchovideoscopes recalled for clarified instructions on therapy equipment

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type 1T180 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 1T180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0029-2026·2025-10-15

    Asiago Texas toast recalled for undeclared milk from cheese and butter

    Harris Teeter is recalling 295 units of its Asiago Texas Toast after finding that cheese and butter were left off the ingredient statement, so milk was not declared.

    Product
    Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris Teeter Raleigh, NC
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Drugs)·D-0094-2026·2025-10-15

    NAD+ injection recalled after elevated endotoxin levels found in one lot

    GenoGenix is recalling NAD+ for Injection at 100 mg/mL and 200 mg/mL from one lot for microbial contamination of sterile products, with elevated endotoxin levels.

    Product
    NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide