The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

9276–9300 of 29156

  • SevereNHTSA·20V510000·2020-08-27

    Vac-Tron Recalls 140 Trucks for Rear Extremity Safety Defect

    Vac-Tron is recalling 140 trucks because the rear extends too far, increasing injury risk in rear-end crashes.

    Product
    VAC-TRON — VAC-TRON JTV 873 PTO, HTV 373 PTO, HTV 873 PTO, HTV 573 PTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V518000·2020-08-27

    Kia Stinger recalled for engine compartment fire hazard

    Kia is recalling certain 2018-2021 Stinger vehicles due to risk of engine compartment fire in the antilock brake control unit. Owners should park outside and away from structures until the fuse kit replacement is completed.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2821-2020·2020-08-26

    Arjo Huntleigh Recalls Citadel Plus Bariatric Bed Frames Due to Melting Cables

    Arjo Huntleigh is recalling 145 Citadel Plus Bariatric Bed Frame Systems because Modular Junction Box cables can melt, potentially affecting bed functionality.

    Product
    Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1282-2020·2020-08-26

    Kroger Recalls Deli Jarlsberg Jalapeno Dip for Salmonella Risk

    The Kroger Co is recalling Deli Jarlsberg Jalapeno Dip in plastic tubs due to potential contamination with Salmonella Newport.

    Product
    DELI JARLSBERG JALAPENO DIP in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1289-2020·2020-08-26

    Kroger Deli Buffalo Blue Cheese Spread Kit Recalled for Salmonella Risk

    The Kroger Co is recalling Deli Buffalo Blue Cheese Spread Kits due to potential contamination with Salmonella Newport. The product was distributed in 20 states.

    Product
    DELI BUFFALO BLUE CHEESE SPREAD KIT in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1280-2020·2020-08-26

    Kroger Recalls AFIN Jarlsberg Cheese Spread Kits for Salmonella Risk

    The Kroger Co is recalling AFIN Jarlsberg Cheese Spread Kits due to potential contamination with Salmonella Newport. The products were distributed in 20 states.

    Product
    AFIN JARLSBERG CHEESE SPREAD KIT in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1160-2020·2020-08-26

    Earth Grown Mocha Fudge Frozen Dessert Recalled for Undeclared Cashews

    Smith Foods Inc. is recalling Earth Grown Mocha Fudge Non-Dairy Frozen Dessert due to undeclared cashews, a major food allergen.

    Product
    Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-1291-2020·2020-08-26

    Kroger Deli Ranch Cheese Spread Kit Recalled for Salmonella Risk

    The Kroger Co is recalling Deli Ranch Cheese Spread Kits due to potential contamination with Salmonella Newport. The products were distributed in 20 states.

    Product
    DELI RANCH CHEESE SPREAD KIT in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereNHTSA·20V500000·2020-08-24

    ETI Recalls 2020 Aerial Lift Trucks Due to Boom Tube Weld Defects

    Equipment Technology is recalling 2020 ETI ETC 37 IH aerial lift trucks because improper welds and steel thickness may cause the platform to fall unexpectedly.

    Product
    ETI — ETI ETC 37 IH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V499000·2020-08-24

    Oshkosh Recalls 2020 S-Series Vehicles for Brake Switch Defect

    Oshkosh is recalling 172 2020 S-Series vehicles because a pressure switch defect may cause air leaks, increased braking distance, or brake light failure.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V496000·2020-08-21

    Autocar Recalls 2019 Xpeditor Vehicles for Potential Stalling Hazard

    Autocar is recalling 78 model year 2019 Xpeditor vehicles up-fitted with an aftermarket power take off (PTO) because they may stall or hesitate, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E057000·2020-08-20

    Motorcar Parts Recalls Duralast Brake Master Cylinders for Volkswagen Models

    Motorcar Parts of America is recalling specific Duralast brake master cylinders for Volkswagen vehicles due to a defect that may cause loss of braking.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1146-2020·2020-08-19

    Island Spring Organics Tofu Recalled Due to Metal Fragment

    Island Spring Inc is recalling 120 cases of Extra Firm Organic Tofu because a customer found a metal fragment in the product.

    Product
    Island Spring Organics Extra Firm Organic Tofu, brand iXF-W12. Product is packaged in small square shapes into vacuum sealed pouches, net wt. 12 oz. Product is refrigerated. UPC is 0 74899 00006 9. The product label is read in parts: "***ISLAND SPRING ORGANICS Extra Firm Tofu*
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1147-2020·2020-08-19

    Wellements Iron Drops Recalled for Undeclared Milk Allergen

    Wellements LLC is recalling Iron Drops liquid dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.

    Product
    Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E056000·2020-08-19

    Tong Yang Recalls Grille Mouldings for 2019-2020 Honda HR-V Vehicles

    Tong Yang is recalling aftermarket grille mouldings for 2019-2020 Honda HR-Vs because the coating may interfere with the Adaptive Cruise Control radar sensor, increasing crash risk.

    Product
    STRUCTURE:BODY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2795-2020·2020-08-19

    Bioseal Trachea Extenders Recalled for Stress Cracks and Leakage Risk

    Bioseal Corporation is recalling 900 units of Trachea Extenders due to stress cracks that may cause breathing system leakage, potentially preventing prescribed ventilation from reaching patients.

    Product
    Bioseal Trachea Extender 1/pl 50pk/Cs, REF TRAX01/50, LOT XXXX, STERILE EO, Single Use Only, Date of Manufacture XXXX, Expiration Date XXXX, LF, UDI: (01) 00630094916019 - Product Usage: Airway connectors intended to connect a breathing gas source to a tracheal tube, tracheostomy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2794-2020·2020-08-19

    Philips HeartStart MRx Monitor/Defibrillators Recalled for Therapy Switch Failure

    Philips is recalling HeartStart MRx monitor/defibrillators because a therapy switch failure may prevent the device from delivering the intended shock energy or function.

    Product
    Philips HeartStart MRx, Monitor/Defibrillators with model numbers M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9 - Product Usage: is intended for use in hospital and pre-hospital settings by qualified medical personnel tra
    Category
    Medical Device
    Distribution
    0 states