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.

176–200 of 29054

  • SevereCPSC·26668·2026-08-06

    Liuqibax Adult Bed Rails Recalled Due to Entrapment and Asphyxiation Risks

    Liuqibax is recalling approximately 12,000 adult portable bed rails sold on Amazon because they violate mandatory safety standards and pose entrapment and asphyxiation hazards.

    Product
    Liuqibax Adult Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26661·2026-08-06

    Attic Stairway Ladders Recalled Over Bolt Break Fall Hazard

    Louisville Ladder is recalling over 1.7 million attic stairway ladders because the bolts can break during use, creating a fall hazard. Eleven reports of bolt breakage have been received, including one injury.

    Product
    Louisville, Featherlite, Lite & Century Attic Stairway Ladders with gas struts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26665·2026-08-06

    Wnttmt Baby Walkers Recalled Due to Fall and Entrapment Hazards

    Wnttmt-branded infant walkers are being recalled because they pose serious injury or death risks from falls and entrapment. These products were sold on Amazon by WURUI.BABY.

    Product
    Wnttmt Baby Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V518000·2026-08-06

    Jayco Recalls 2027 Fifth Wheel Trailers Due to Auto Leveling Jack Defect

    Jayco is recalling 2027 Eagle and Heartland Sundance fifth wheel trailers because auto leveling jacks may lower during transit, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, HEARTLAND EAGLE, SUNDANCE FIFTH WHEEL, EAGLE SLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V517000·2026-08-06

    Isuzu NPR HD Liftgate Deck Pin Recall

    US Truck Body is recalling 2025 Isuzu NPR HD vehicles with Waltco liftgates because deck pins may break, causing the platform to fall.

    Product
    ISUZU — ISUZU NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26671·2026-08-06

    Little Rawr Silicone Pull String Teething Toys Recalled Due to Choking Hazard

    Little Rawr Silicone Pull String Teething Toys are being recalled because the silicone strings are too long and thin, posing a choking and respiratory distress risk. One report of a child experiencing respiratory distress has been received.

    Product
    Little Rawr Silicone Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2807-2026·2026-08-05

    Medtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77522

    Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.

    Product
    EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2819-2026·2026-08-05

    Medical Convenience Kits Recalled Over Lidocaine Injection Supplier Quality Issues

    Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray - RX, Part Number 008786-19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2809-2026·2026-08-05

    Medtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77722

    Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.

    Product
    EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V505000·2026-08-04

    Escape Recalls 2025-2026 E13 F1 Trailers Due to Carbon Monoxide Risk

    Escape Trailer Industries is recalling 2025-2026 E13 F1 recreational trailers because insufficient refrigerator ventilation may allow carbon monoxide to build up inside the cabin.

    Product
    ESCAPE — ESCAPE ESCAPE 13
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2026·2026-07-31

    Baked spaghetti and chicken cobbler recalled for possible metal fragment contamination

    Ukrop's Homestyle Foods recalled about 22,880 pounds of baked spaghetti and chicken cobbler that may contain metal slivers. FSIS classified it Class I. No confirmed injuries.

    Product
    Ukrop's Homestyle Foods — Ukrop's Homestyle Foods Recalls Spaghetti and Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·26632·2026-07-30

    TT Trsmima zipline kits and spring brakes recalled for fall and collision hazards

    TT Trsmima backyard zipline kits and spring brakes can break, detach or fail to slow riders. Reports include fractures, concussions, sprains and abrasions across two separate failure modes.

    Product
    TT Trsmima Zipline Kits and Zipline Spring Brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V494000·2026-07-30

    2026 Cadillac, GMC, and Chevrolet electric vehicles recalled due to battery fire risk

    General Motors is recalling certain 2026 Cadillac Escalade, GMC Sierra EV, and Chevrolet Silverado EV models because an improperly secured battery component may increase the risk of a fire.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SILVERADO EV, ESCALADE IQ, ESCALADE IQL, SIERRA EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V500000·2026-07-30

    Honda Motorcycles Recalled Due to Handlebar Lock Screw Risk

    Honda is recalling certain CMX300, CMX500, and SCL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.

    Product
    HONDA — HONDA SCL500, CMX500, CMX300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V498000·2026-07-30

    Winnebago Ekko Motorhomes Recalled Over Generator Software Fault

    Winnebago is recalling certain 2024-2025 Ekko motorhomes because the touchscreen display may register unintended inputs and turn the generator on without the operator's knowledge.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V497000·2026-07-30

    Wanco Recalls Compact Light Towers Due to Fuel Tank Leak Risk

    Wanco is recalling 2025-2026 Compact Light Towers because the diesel fuel tank may crack and leak, increasing fire risk.

    Product
    WANCO — WANCO COMPACT LIGHT TOWER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V496000·2026-07-30

    GM Recalls 2026 Silverado and Sierra EVs for Wheel Cracking Risk

    General Motors is recalling 2026 Chevrolet Silverado EV and GMC Sierra EV vehicles because steel wheels may crack, potentially causing loss of control.

    Product
    GMC — GMC, CHEVROLET SIERRA EV, SILVERADO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26652·2026-07-30

    OCTROT heated throws and blankets recalled after 27 fires and injuries

    About 178,000 OCTROT electric throws and blankets can have their cord detach and ignite. The firm reports 555 incidents resulting in 27 fires and 15 burn or electrical shock injuries.

    Product
    OCTROT Electric Thows and Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0703-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 88 mcg, lot N02310, due to subpotency. The recall is voluntary and affects nationwide distribution in the USA.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2764-2026·2026-07-29

    Medline Medical Procedure Convenience Kits Recalled Due to Potential Drug Ineffectiveness

    Medline Industries, LP is recalling certain MEDLINE medical procedure convenience kits because they contain ICU Medical, Inc. pain management kits that may be ineffective.

    Product
    MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2765-2026·2026-07-29

    MEDLINE Medical Procedure Kits Containing Bupivacaine Recalled Due to Drug Ineffectiveness

    Medline Industries is recalling 318 medical procedure kits that contain ICU Medical pain management kits with Bupivacaine Hydrochloride in Dextrose Injection due to quality issues that could result in drug ineffectiveness.

    Product
    MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T; 2) TOTAL KNEE-LF, Medline kit SKU CDSOPT590U; 3) TOTAL KNEE CDS, Medline kit SKU CDS983930J; 4) HIP CDS-LF, Medline kit SKU CDS984556L; 5) HIP CDS-LF, Medline kit SKU CDS9845
    Category
    Medical Device
    Distribution
    3 states