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.

5601–5625 of 29102

  • SevereNHTSA·23E022000·2023-03-20

    Meritor Recalls Front Drive Steer Axles Due to Loose Fasteners

    Meritor is recalling specific front drive steer axles because fasteners may not be tightened sufficiently. This defect could cause axle separation and loss of vehicle control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V178000·2023-03-17

    Mercedes-Benz Recalls GLE and GLS Models for Rear Window Trim Defect

    Mercedes-Benz is recalling 70,225 GLE and GLS vehicles because rear door window trim bars may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLS63 4MATIC+, GLS 580 4MATIC, GLS 450 4MATIC, AMG GLE63 S 4MATIC+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2023·2023-03-17

    WOW Frozen Food Recalls Uninspected Frozen Meat and Poultry Sfihas

    WOW Frozen Food LLC is recalling approximately 488 pounds of frozen sfihas products produced without federal inspection. The items were sold in Florida and via Instagram.

    Product
    WOW Frozen Food LLC Recalls Frozen Meat and Poultry Sfihas Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·008-2023·2023-03-17

    Hoyo Recalls Frozen Beef Sambusa Due to Possible Metal Contamination

    Hoyo, SBC is recalling approximately 1,046 pounds of frozen beef sambusa products due to possible contamination with thin, wire-like metal.

    Product
    Hoyo, SBC — Hoyo, SBC Recalls Frozen, Ready-To-Eat Beef Sambusa Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V177000·2023-03-17

    Mercedes-Benz Recalls GLE and GLS Models for Fire Risk

    Mercedes-Benz is recalling certain 2020-2021 GLE and GLS models because incorrectly installed air conditioner drain hoses may cause water intrusion, increasing the risk of fire or electrical failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE63, GLE 580, MAYBACH GLS600, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V172000·2023-03-16

    2023 Cadillac XT6 Transmission Defect Recall for Half-Shaft Disengagement

    General Motors is recalling 2023 Cadillac XT6 and related vehicles due to a transmission defect. An incorrectly built sun gear can cause the half-shaft to disengage, risking loss of drive power or vehicle rollaway.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC XT5, BLAZER, XT6, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E021000·2023-03-16

    Ducati Recalls Desert X Soft Side Bags Due to Fire Risk

    Ducati is recalling 65 Desert X Soft Side Bags Kits because the right-side bag may contact the exhaust, posing a fire and crash risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23734·2023-03-16

    Polaris Sportsman ATVs Recalled for Fire and Brake Loss Hazards

    Polaris is recalling model years 2021–2023 Sportsman 450 and 570 ATVs because an improperly assembled wiring harness can contact the brake line and vehicle frame, resulting in front brake loss and fire.

    Product
    Model Years 2021-2023 Sportsman 450 and 570 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0411-2023·2023-03-15

    JSJ ZSR Cake recalled for undeclared egg allergen

    Titans Global Inc. is recalling JSJ ZSR Cake due to undeclared egg on the label. The recall affects 12,432 units distributed to five retail locations in California.

    Product
    JSJ ZSR Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1145-2023·2023-03-15

    Cardiosave Hybrid IABP Devices Recalled for Unexpected Shutdown Risk

    Datascope Corp. is recalling Cardiosave Hybrid IABP devices due to a connection failure that may cause unexpected shutdown during use. The failure prevents communication between the device's display head and base unit.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1146-2023·2023-03-15

    Cardiosave Rescue Intra-Aortic Balloon Pumps recalled for connection failure

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to a coiled cord cable connection failure that may cause unexpected device shutdown and loss of communication.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V167000·2023-03-15

    2023 Alliance RV Valor travel trailers recalled for incorrect wheel assemblies

    Alliance RV is recalling certain 2023 Valor 21T15 travel trailers with incorrect wheel and tire assemblies that may become overloaded. Overloaded tires can fail and increase the risk of crashes.

    Product
    ALLIANCE RV — ALLIANCE RV VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0412-2023·2023-03-15

    JSJ DMC Leaf Cake recalled due to undeclared egg allergen

    JSJ DMC Leaf Cake (3.35 oz, produced 2022/11/08) has been recalled because egg is present but not declared on the label. The recall affects 12,432 units distributed to 5 retail locations in California.

    Product
    JSJ DMC Leaf Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0410-2023·2023-03-15

    JSJ Chocolate Cake Recalled for Undeclared Egg Allergen

    Titans Global Inc. is recalling JSJ Chocolate Cake due to undeclared egg not listed on the label. The recall affects 12,432 units distributed to five retail locations in California.

    Product
    JSJ Chocolate Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1147-2023·2023-03-15

    Cardiosave Hybrid IABP Recalled for Risk of Unexpected Shutdown

    The Cardiosave Hybrid intra-aortic balloon pump (IABP) is being recalled because it may unexpectedly shut down due to communication loss between internal components. The shutdown could interrupt therapy in cardiac patients and compromise their hemodynamic stability.

    Product
    Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998-UC-0800-52* 0998-UC-0800-53* 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0456-2023·2023-03-15

    Drug Recall: Pharmedica Non-Sterile MSM Drops Due to Contamination

    Pharmedica USA recalled Purely Soothing 15% MSM Drops nationwide due to non-sterility concerns. The voluntary Class I recall affects approximately 1,904 bottles distributed via e-commerce and trade shows.

    Product
    Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0417-2023·2023-03-15

    Chukar Cherries Cherry Bombs Recalled Nationwide for Undeclared Hazelnuts

    Chukar Cherry Company is recalling Cherry Bombs Bits 'n Pieces chocolate candy nationwide due to undeclared hazelnuts, a food allergen.

    Product
    Chukar Cherries Cherry Bombs Bits 'n Pieces, item #21508, net wt. 12 oz. (340g). UPC 0 11261 21508 9. Product is packaged in clear plastic film pouch. INGREDIENTS: Milk, Bittersweet, Semisweet, and White Chocolate (Sugar, Unsweetened Chocolate processed with potassium carbonate
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23735·2023-03-09

    Bedsure Electric Heating Blankets and Pads Recalled for Fire and Burn Hazards

    Bedsure electric heating blankets and pads are recalled because their controllers can malfunction, causing fires and thermal burns. Consumers should stop using them immediately and contact Bedsure for a refund.

    Product
    Bedsure Electric Heating Blankets and Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V150000·2023-03-08

    Terex Advance Mixer Recall: Steering Shaft May Come Loose

    Terex Advance is recalling 2022-2023 Front Discharge Mixers because the steering shaft may come loose, risking loss of steering control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2023·2023-03-08

    PrimeZEN Black 6000 Capsule Recalled for Undeclared Pharmaceutical Ingredients

    The FDA is recalling PrimeZEN Black 6000 capsules distributed nationwide because they contain undeclared sildenafil and tadalafil. The product is unapproved and was marketed without FDA authorization.

    Product
    PrimeZEN Black 6000 capsule, 2000mg, Male Sexual Performance Enhancement, 1-count blister card, Distributed by: Prime Premier Group, Los Angeles, CA 90006, UPC 7 28175 52189 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V152000·2023-03-08

    Bentley Recalls Continental GT Cabrio for Air Bag Defect

    Bentley is recalling 2020-2021 Continental GT Cabrio vehicles because a sharp edge on the air bag deflector bracket may cause seat air bags to tear during deployment.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT CABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0384-2023·2023-03-08

    Matsunaga Mini Shiruko Sand Biscuits Recalled Due to Undeclared Soy Allergen

    Matsunaga Mini Shiruko Sand Biscuits are being recalled because they contain soy allergen that is not listed on the ingredient label. Consumers with soy allergies should not consume this product.

    Product
    Matsunaga Mini Shiruko Sand Biscuits 100 g packages, containing 4 individually wrapped servings of 4 (25mg per unit) SKU number 4902773016966 Manufactured in Japan.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1141-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Patient Desaturation Risk

    Baxter Healthcare is recalling 8 Life2000 Hospital Ventilator systems due to potential patient desaturation events when the device is connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide