The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

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351–375 of 26079

  • SevereNHTSA·24V381000·2026-06-05

    2022-2023 Toyota Tundra and Lexus LX engine failure recall

    Manufacturing debris may contaminate the V35A engine in certain 2022-2023 Toyota Tundra and Lexus LX600 vehicles, causing bearing failure, stalling, and power loss that increases crash risk.

    Product
    TOYOTA — 2022 TOYOTA TUNDRA
    Category
    Vehicle
    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·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
  • 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
  • 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·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
  • HighNHTSA·25V263000·2026-06-04

    2025 East to West Bravado Motorhome Floor Detachment and Seatbelt Defect

    Forest River is recalling 2025 East to West Bravado motorhomes because the slide-room floor may detach and fail to properly retain seatbelts during a crash. Dealers will secure the floor at no cost.

    Product
    EAST TO WEST — 2025 EAST TO WEST BRAVADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V188000·2026-06-04

    2025 Nissan Kicks: Certification labels with incorrect weight and tire ratings

    Certain 2025 Nissan Kicks vehicles have certification labels with incorrect Gross Vehicle Weight Rating and Gross Axle Weight Rating values, which could lead to vehicle overloading and crash risk. Some SR trim vehicles with an optional 19-inch wheel package also have incorrect tire size information.

    Product
    NISSAN — 2025 NISSAN KICKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V218000·2026-06-04

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    GENESIS — 2024 GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26526·2026-06-04

    Children's Tiny Land Play Tents Recalled for Skin and Eye Irritation Risk

    Tiny Land Inc. is recalling about 7,500 children's play tents because fiberglass poles can shed fibers, causing skin and eye irritation. Consumers should stop using the tents immediately and contact Tiny Land for a free repair kit with plastic replacement poles.

    Product
    Children's Tiny Land Play Tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26530·2026-06-04

    Boon NURSH 8 oz Reusable Baby Bottles Recalled for Choking Hazard

    TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.

    Product
    Boon NURSH 8 oz Reusable Baby Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V264000·2026-06-04

    Coachmen Catalina travel trailers recalled for improper electrical wiring

    Forest River is recalling 2024-2025 Coachmen Catalina and Forest River Aurora travel trailers due to improper wiring and inadequate circuit protection on accent lights and auto-leveling systems. The defect poses an electrical fire risk.

    Product
    COACHMEN — 2025 COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26528·2026-06-04

    Gudook Adult Bike Helmets Recalled for Serious Head Injury Risk

    Gudook Adult Bike Helmets (model KY-055, batch 202503, March 2025 manufacture) violate mandatory safety standards and fail to protect users in a crash, posing a serious risk of head injury or death. About 520 units sold on Amazon from May 2025 through February 2026.

    Product
    Gudook Adult Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2235-2026·2026-06-03

    Medline spinal anesthetic kits recalled for quality and efficacy concerns

    Medline Industries is recalling 4,370 spinal anesthetic kits due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2234-2026·2026-06-03

    Medline anesthetic injection kits recalled for quality and efficacy concerns

    Medline has recalled 270 bupivacaine injection kits due to microbiology testing data integrity concerns and reported efficacy complaints. The FDA classified this as a Class I recall.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0857-2026·2026-06-03

    Wawa Diet Lemonade Recalled for Undeclared Milk Allergen

    Wawa recalls Diet Lemonade Pint bottles for undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    Wawa Diet Lemonade Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0850-2026·2026-06-03

    Butter Parsley Bagel Crisps Recalled Due to Salmonella Contamination

    Legacy Bakehouse LLC is recalling Butter Parsley Bagel Crisps due to Salmonella contamination from recalled milk powder. The affected products were distributed in Pennsylvania and Wisconsin.

    Product
    Butter Parsley Bagel Crisps, Item Number 18490, 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

    Honeyville Bulk Banana Smoothie Product Recalled Due to Salmonella Risk

    Honeyville, Inc. is recalling a bulk banana smoothie product due to potential Salmonella contamination from an ingredient used in manufacturing. Distribution was to California and Utah.

    Product
    (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0855-2026·2026-06-03

    Wawa Iced Tea Lemon Recalled for Undeclared Milk Allergen

    Wawa Iced Tea Lemon 16 oz bottles are recalled due to undeclared milk allergen. The product was distributed in Delaware, Maryland, New Jersey, Pennsylvania, and Virginia.

    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 kits recalled for bupivacaine quality issues

    Medline is recalling spinal anesthesia kits containing Huons bupivacaine hydrochloride due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints. Affected kits were distributed worldwide.

    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 Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2233-2026·2026-06-03

    Medline Spinal Trays Recalled Due to Quality and Efficacy Concerns

    Medline Industries is recalling 41,720 spinal anesthesia trays containing Bupivacaine due to quality issues, microbiology testing data integrity concerns, and reported efficacy complaints affecting patient safety.

    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 T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0856-2026·2026-06-03

    Wawa Diet Iced Tea Lemon Recalled for Undeclared Milk Allergen

    Wawa is recalling Diet Iced Tea Lemon in 16oz bottles due to undeclared milk allergen that may affect consumers with milk allergies. Bottles were distributed across five states.

    Product
    Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2236-2026·2026-06-03

    Medline spinal injection kits recalled for quality and efficacy concerns

    Medline Industries recalls 30,120 spinal injection kits containing Huons Bupivacaine due to quality control failures and reported efficacy complaints. The FDA Class I recall affects kits distributed in the US and selected territories.

    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

    Parmesan & Herb Bagel Crisps Recalled for Salmonella Risk

    Parmesan & Herb Bagel Crisps from Legacy Bakehouse LLC are being recalled due to Salmonella contamination from a recalled milk powder ingredient. Affected product was distributed in Pennsylvania and Wisconsin.

    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