The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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.

876–900 of 32252

  • SevereNHTSA·26V369000·2026-06-09

    Ford Recalls 2012-2018 Focus Vehicles for Engine Stall Risk

    Ford is recalling 2012-2018 Focus vehicles previously repaired under recall 18V735 because a malfunctioning Canister Purge Valve may cause the engine to stall while driving, increasing crash risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E033000·2026-06-09

    Cummins CNG Fuel System Recall for Tank Bracket Deformation Risk

    Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V378000·2026-06-09

    Ford Recalls 2014 F-150s for Transmission Software Update

    Ford is recalling 2014 F-150 vehicles previously repaired under recall 24V444 because a signal loss can cause unexpected downshifting, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V371000·2026-06-09

    Ford Recalls 2024 Explorers for Potential Park System Damage

    Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26525·2026-06-04

    Little Grape Land Nursing Pillows Recalled Due to Suffocation Risk

    Little Grape Land Nursing Pillows are being recalled due to a risk of serious injury or death from suffocation. The pillows violate mandatory safety standards for nursing pillows and infant support cushions. No injuries have been reported.

    Product
    Little Grape Land Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26532·2026-06-04

    Vornado SRTH Small Room Tower Heaters Recalled for Fire Hazard

    Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.

    Product
    SRTH Small Room Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26524·2026-06-04

    Wyze Solar Cam Pan Security Cameras recalled for fire and burn hazard

    Wyze Labs is recalling about 321,360 Solar Cam Pan security cameras because incorrect assembly instructions can cause the lithium-ion battery to overheat and catch fire. The firm has received 13 reports of overheating, six of fires, and six reports of minor burns.

    Product
    Wyze Solar Cam Pan Security Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26529·2026-06-04

    Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Broqixin pool drain covers violate federal safety standards and pose a risk of serious injury or death from entrapment and drowning. About 370 units sold on Amazon from January to April 2026 should be removed immediately.

    Product
    Broqixin Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26531·2026-06-04

    Residential Elevator Interlock Switches Recalled for Fall and Crushing Hazard

    SUNS International is recalling about 7,000 SS6291 Solenoid Interlock Switches used in residential elevators because they can become stuck, allowing the exterior door to remain unlocked and creating a risk of death or serious injury.

    Product
    SUNS SS6291 Solenoid Interlock Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V363000·2026-06-04

    Jeep Recalls Wrangler and Gladiator Models Due to Fire Risk

    Chrysler is recalling 2021-2025 Jeep Wrangler and Gladiator vehicles because steering pump wiring may overheat and cause a fire.

    Product
    JEEP — JEEP GLADIATOR, WRANGLER, WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26527·2026-06-04

    Crenlux Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.

    Product
    Crenlux Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2236-2026·2026-06-03

    Medline spinal block trays recalled over Huons bupivacaine quality concerns

    Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0851-2026·2026-06-03

    Legacy Bakehouse parmesan herb bagel crisps made with recalled milk powder

    Parmesan & Herb Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    Parmesan & Herb Bagel Crisps, Item Number 18139, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0849-2026·2026-06-03

    Bulk banana smoothie base made with potentially Salmonella-contaminated ingredient

    A bulk banana smoothie base is being recalled because the firm received and used a potentially Salmonella-contaminated ingredient to manufacture various products. 4,980 pounds are affected.

    Product
    (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0857-2026·2026-06-03

    Wawa diet lemonade pints recalled over undeclared milk allergen

    Wawa Diet Lemonade in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 374 units are affected.

    Product
    Wawa Diet Lemonade Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2233-2026·2026-06-03

    Medline spinal trays recalled over Huons bupivacaine quality concerns

    Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0858-2026·2026-06-03

    Wawa fruit punch pints recalled over undeclared milk allergen

    Wawa Fruit Punch in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 1,694 units are affected.

    Product
    Wawa Fruit Punch Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0855-2026·2026-06-03

    Wawa Iced Tea Lemon 16 oz Pint Recalled Due to Undeclared Milk

    Wawa Beverage Company is recalling Wawa Iced Tea Lemon 16 oz Pint plastic bottles because they contain undeclared milk.

    Product
    Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2237-2026·2026-06-03

    Medline spinal anesthesia trays recalled over Huons bupivacaine quality concerns

    Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2232-2026·2026-06-03

    Medline pain and Whitacre spinal trays recalled over bupivacaine concerns

    Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817; 3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920; 4) ULTRASOUND…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2160-2026·2026-06-03

    RelayPro thoracic stent-graft clasp may not release from delivery system

    The RelayPro Thoracic Stent-Graft System is subject to a labeling update concerning proximal clasp disconnection from the outer control tube, which may prevent release of the graft.

    Product
    RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U…
    Category
    Medical Device
    Distribution
    1 state