The Recall Desk

Hazard

Class I recalls

702 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all class i recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

551–575 of 702

  • SevereFDA (Devices)·Z-2291-2025·2025-08-20

    HeartMate mobile power unit cords may disconnect from a misaligned lock

    HeartMate Mobile Power Units are being recalled because misaligned V-Lock features on the power cords prevent the locking mechanism engaging properly and may cause unintended disconnect. 604 units affected.

    Product
    Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2228-2025·2025-08-20

    DreamStation Auto BiPAP units may hold an incorrect device configuration

    DreamStation Auto BiPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 8 units are affected.

    Product
    DreamStation Auto BiPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2227-2025·2025-08-20

    DreamStation Auto CPAP units may hold an incorrect device configuration

    DreamStation Auto CPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 57 units are affected.

    Product
    DreamStation Auto CPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0473-2025·2025-08-20

    Ready Meals duo tuna salad with crackers recalled over Listeria risk

    Ready Meals Duo Tuna Salad with Crackers is being recalled because of potential contamination with Listeria monocytogenes. The source does not state a quantity.

    Product
    READY MEALS DUO TUNA SALAD W/ CRACKERS
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-2129-2025·2025-08-13

    Plum Duo infusion system interface may become unresponsive during programming

    The Plum Duo Infusion System is being recalled because two sequences of programming events and alarm interactions may cause the user interface to become unresponsive. 4,677 units are affected.

    Product
    Plum Duo Infusion System, List Number: 400020401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0379-2025·2025-08-13

    Bulk pecan pieces and halves recalled over potential Salmonella contamination

    Bulk pecan pieces and halves are being recalled because the pecans have the potential to be contaminated with Salmonella. 32,670 lbs are affected.

    Product
    FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 SDC1645 90 FANCY MEDIUM PECAN PIECES 81124 561965 554714 6/13/2025 SDC1645 90 FANCY MIDGET PECAN PIECES 81086 561845 554594 5/30/2025 SDC1505 56 FCY #15 HLVS 79291 561943 554692 5/21/2025 SDC1405 56 FANCY SMALL PECAN PIECES
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0387-2025·2025-08-13

    Parashore pear slices contaminated with elevated lead and cadmium

    Parashore Pear Slices in Juice, 15 oz, are being recalled because the product is contaminated with elevated lead and cadmium. 8,160 units are affected.

    Product
    Parashore Pear Slices in Juice, 15 oz. (425 g), UPC#704817164237
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2176-2025·2025-08-13

    Microbore extension sets are labeled as having an air eliminating filter

    Microbore Extension Sets with 0.2 Micron Filter are being recalled because the label indicates an air eliminating filter, but the filter fitted is not indicated for air removal. 34,825 US units affected.

    Product
    Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
    Category
    Medical Device
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2182-2025·2025-08-13

    BritePro Solo mini handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Mini Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02-0130U (Mac 3), 040-02-0131U (Mac 3 Strong Curve) 040-02-0140U (Mac 4), 040-02-0400U (Miller 00), 040-02-0410U (Miller 1), 040-02-0420U (Miller 2), 040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2186-2025·2025-08-13

    BritePro Solo mini laryngoscope handles may not illuminate as intended

    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0419-2025·2025-08-13

    Italian layer cake recalled because its pecans may carry Salmonella

    Item #1071 Italian layer cake is being recalled because the pecans used in it have the potential to be contaminated with Salmonella. The source does not state a quantity.

    Product
    Item #1071 Italian layer cake
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2183-2025·2025-08-13

    BritePro Solo laryngoscope handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac 1), 040-332U (Mac 2), 040-333U (Mac 3), 040-335U (Mac 3.5) 040-334U (Mac 4), 040-341U (Miller 1), 040-342U (Miller 2), 040-343U (Miller 3), 040-344U (Miller 4), 040-361U (Phillips 1), 040-36
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2185-2025·2025-08-13

    BritePro Solo stubby laryngoscope handles may not illuminate as intended

    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2187-2025·2025-08-13

    BritePro Solo fiber optic laryngoscope handles may not illuminate properly

    BritePro Solo Single-Use Fiber Optic Laryngoscope Handles, REFs 040-310AU and 040-310U, are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0394-2025·2025-08-13

    Member's Mark freeze dried fruit packs tested positive for Listeria monocytogenes

    Member's Mark Freeze Dried Fruit Variety Pack 15 count is being recalled after the firm received positive test results for Listeria monocytogenes during routine testing. 21,552 boxes affected.

    Product
    Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-2180-2025·2025-08-13

    BD Alaris pump infusion sets may perform outside established flow ranges

    BD Alaris Pump Infusion Sets are being recalled because the pump module used with them may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2452-0007, BD Alaris Pump Infusion Set, 2 Back Check Valves, 3 SmartSite Y-sitesAS LVP 10D 3SS 2CV; REF: 2204-0007, BD Alaris Pum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2179-2025·2025-08-13

    BD Alaris pump modules may perform outside established flow rate ranges

    BD Alaris Pump Module Model 8100 with Guardrails Suite MX software is being recalled because it may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0391-2025·2025-08-13

    Aral Silver Vobla dried roach fish recalled over Clostridium botulinum risk

    Aral Silver Vobla whole dried salted roach fish is being recalled because of Clostridium botulinum in uneviscerated fish. 23 boxes are affected across sixteen states.

    Product
    ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole eviscerated dried roach fish, caviar may be present, salt.; Distributed by Krasnyi Oktyabr; PERISHABLE KEEP REFRIGERATED AT OR BELOW 40F; PRODUCT OF KAZAKHSTAN
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-2184-2025·2025-08-13

    BritePro Solo mini Miller blade handles may not illuminate as intended

    BritePro Solo Mini with Pro Miller Blade Size 1.5 is being recalled because the laryngoscope handles may not illuminate as intended.

    Product
    BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U
    Category
    Medical Device
    Distribution
    Distributed nationwide