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.

8576–8600 of 29123

  • SevereFDA (Drugs)·D-0266-2021·2021-03-03

    CareFusion Recalls Non-Sterile ChloraPrep Solution Due to Microbial Contamination Risk

    CareFusion 213, LLC is recalling non-sterile ChloraPrep With Tint solution distributed in Puerto Rico and Oman due to potential fungal contamination.

    Product
    ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution - Hi-Lite Orange, 0.10 fl. oz. (3 ml) each, 25 applicators in carton, CareFusion El Paso, TX 79912, NDC 054365-400-11 Cat. No. 260415
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0271-2021·2021-03-03

    Teva Recalls Dacarbazine Injection Due to Sterility Assurance Concerns

    Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.

    Product
    Dacarbazine for Injection USP, 200 mg, Single Use Vial (NDC 0703-5075-01), packaged in 10X20 ML Single Use Vials per tray (NDC 0703-5075-03); Rx only, TEVA Pharmaceuticals USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0322-2021·2021-03-03

    Thai Peanut Sauce Recalled for Undeclared Shrimp Allergen

    Barbara's Orchard/Delicae Gourmet is recalling Thai Peanut Sauce due to undeclared shrimp. Consumers should stop using the product and return it to the store.

    Product
    Thai Peanut Sauce, 12 fl. oz. (355ml), UPC code #643558406919
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0321-2021·2021-03-03

    Spicy Red Curry Sauce Recalled for Undeclared Shrimp Allergen

    Barbara's Orchard/Delicae Gourmet is recalling Spicy Red Curry Sauce due to an undeclared shrimp allergen. Consumers should check their pantry for the affected batches.

    Product
    Spicy Red Curry Sauce, 12 fl. oz. (355ml), UPC code #643558406810
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1138-2021·2021-03-03

    DeRoyal Recalls Non-Sterile Sternum Saw Blades in Surgical Packs

    DeRoyal Industries is recalling 309 CV Basin Set Packs because the included sternum saw blades are not sterile.

    Product
    CV Basin Set Pack, REF numbers: a) 89-7935.11 b) 89-7935.12 c) 89-7935.13 d) 89-7935.14 e) 89-7935.15 f) 89-7935.16 Custom surgical procedure packs including sternum saw blades.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0268-2021·2021-03-03

    FDA Recalls Chloraprep One-Step Antiseptic Due to Non-Sterility Risk

    CareFusion 213, LLC is recalling 400 cartons of Chloraprep One-Step antiseptic applicators distributed in Puerto Rico and Oman due to potential fungal growth and package integrity breaches.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0281-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, 1 mL Single-Dose Vial (NDC 0703-0051-01), packaged in 25X1ML vials per tray (NDC 0703-0051-04), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V130000·2021-03-02

    Ferrara Recalls 2009-2020 Aerial Vehicles Due to Trolley Defect

    Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.

    Product
    FERRARA — FERRARA AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V127000·2021-03-01

    Hyundai Recalls Kona and Ioniq Electric Vehicles for Battery Fire Risk

    Hyundai is recalling 2019-2020 Kona Electric and 2020 Ioniq Electric vehicles because the lithium-ion battery may short-circuit, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI KONA ELECTRIC, IONIQ ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2021·2021-03-01

    Milky Way Recalls Canned Corned Beef Imported Without Inspection

    Milky Way International Trading Corp. is recalling approximately 297,715 pounds of canned corned beef products that were imported and distributed in the U.S. without FSIS import re-inspection.

    Product
    Milky Way International Trading Corp. Recalls Canned Corned Beef Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V123000·2021-02-26

    Mercedes-Benz Recalls 2018 GLE Models Due to Tire Defect

    Mercedes-Benz is recalling 2,529 2018 GLE 350, GLE 400, and AMG GLE43 vehicles because over-cured tires may fail, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 400, AMG GLE43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V122000·2021-02-26

    KTM Recalls 2020 1290 Super Duke R Motorcycles for Wiring Harness Defect

    KTM is recalling 2020 1290 Super Duke R motorcycles because an incorrectly routed rear wiring harness could cause an electrical short-circuit, leading to engine stalling and increased crash risk.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2021·2021-02-26

    J&J Distributing Recalls Ready-to-Eat Meat and Poultry Salads and Wraps

    J&J Distributing is recalling ready-to-eat meat and poultry salads and wraps due to possible Listeria monocytogenes contamination.

    Product
    J&J Distributing — J&J Distributing Recalls Ready-to-Eat Meat and Poultry Salads and Wrap Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·21V120000·2021-02-25

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Engine Software Defect

    Daimler Trucks North America is recalling 2019-2021 Thomas Built Buses Saf-T-Liner C2 school buses because engine software may fail to limit speed or torque, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V119000·2021-02-25

    Vermeer Recalls 2021 BC900XL Trailers Due to Axle Bolt Issue

    Vermeer is recalling 2021 BC900XL brush chipper trailers because axle mounting bolts may not be tightened properly, increasing crash risk.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V115000·2021-02-25

    GM Recalls 33,838 Vehicles Due to Over-Cured Continental Tires

    General Motors is recalling 33,838 vehicles equipped with over-cured Continental tires that may develop sidewall breaks or belt separation, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET, CADILLAC YUKON XL, SILVERADO 1500, SAVANA, SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V107000·2021-02-24

    Lamborghini Recalls Aventador SVJ Vehicles Due to Hood Hinge Defect

    Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0295-2021·2021-02-24

    Barron County Organics Recalls Frozen Custard for Pasteurization Failure

    Barron County Organics is recalling 20 Mile Holiday EggNog Organic Frozen Custard because ingredients were not pasteurized after blending as required by Wisconsin state regulations.

    Product
    20 Mile Holiday EggNog, Organic Frozen Custard, Contents: One U.S. Pint and 86 oz. Scoopers. UPC 50005-48815. Made by Barron County Organics, LLC, 10-Mile Organic and Local General Store, 796 29 3/4 Ave. Barronett, WI 54813.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0302-2021·2021-02-24

    Barron County Organics Recalls Frozen Custard Due to Pasteurization Failure

    Barron County Organics is recalling 20 Mile Rhubarb Organic Frozen Custard because ingredients were not pasteurized after blending as required by Wisconsin state regulations.

    Product
    20 Mile Rhubarb, Organic Frozen Custard, Contents: One U.S. Pint and 86 oz. Scoopers. UPC 50005-48811. Made by Barron County Organics, LLC, 10-Mile Organic and Local General Store, 796 29 3/4 Ave. Barronett, WI 54813.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1112-2021·2021-02-24

    Combat Medical Systems Recalls Low Titer Type O FWB Transfusion Sets

    Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.

    Product
    Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V106000·2021-02-23

    Mercedes-Benz Metris Recall for Improperly Welded Front Passenger Seat Frame

    Daimler Vans USA is recalling 2021 Mercedes-Benz Metris vans because the front passenger seat frame base may not have been welded properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide