The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. The hazard can cause serious injury or death. 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 7484

  • 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 (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-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-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…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0050-2026·2025-10-22

    Boxed medium brown eggs recalled over potential Salmonella contamination

    Black Sheep Egg Company is recalling 14,220 dozen Free Range Grade AA Medium Brown Eggs loose packed in boxes for potential Salmonella contamination.

    Product
    Free Range Grade AA Medium Brown Eggs, Loose Pack in Boxes, 15dz per box, 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 (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 (Devices)·Z-0050-2026·2025-10-22

    BF-1TQ170 bronchovideoscopes recalled for updated instructions on laser use

    Olympus is recalling Bronchovideoscope BF-1TQ170 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170
    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-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