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.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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1676–1700 of 114837

  • SevereCPSC·26648·2026-08-06

    DR Power PRO MAX30 Lawn Mowers Recalled Over Blade Control Hazard

    DR Power Equipment is recalling about 320 DR Power PRO MAX30 30-inch walk-behind power lawn mowers because the blade control system can fail, allowing the blades to keep spinning after release and posing a serious laceration hazard.

    Product
    DR Power PRO MAX30 30" Walk-Behind Power Lawn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26676·2026-08-06

    Laziza Dressers Recalled Due to Tip-Over and Entrapment Hazards

    Fitueyes, Inc. is recalling Laziza Dressers because they pose tip-over and entrapment hazards that could cause serious injury or death to children.

    Product
    Laziza Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26663·2026-08-06

    Winston Porter and Seeday Dressers Recalled Due to Tip-Over and Entrapment Hazards

    Winston Porter and Seeday 3-drawer, 4-drawer, and 5-drawer dressers are being recalled because they can tip over or cause entrapment, posing serious injury or death risks to children.

    Product
    Winston Porter and Seeday 3-Drawer, 4-Drawer and 5-Drawer Dressers
    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
  • HighNHTSA·26V512000·2026-08-06

    Toyota Recalls 2026 bZ Woodland Vehicles for Electrical Short Circuit Risk

    Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.

    Product
    TOYOTA — TOYOTA BZ WOODLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26673·2026-08-06

    Mini Laser Pointer Keychains Recalled Due to Battery Ingestion Risk

    KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.

    Product
    Laser & LED Light Mini Laser Pointer Keychains
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26C005000·2026-08-06

    Evenflo Recalls Revolve180 Litemax NXT Child Seats Due to Recline Defect

    Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V516000·2026-08-06

    International Recalls 2027 Trucks Due to Wiper Nut Loosening Risk

    International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.

    Product
    INTERNATIONAL — INTERNATIONAL HX, LT, RH, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26662·2026-08-06

    Easter LED Headbands Recalled Due to Battery Ingestion Risk

    OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.

    Product
    Easter LED Headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26672·2026-08-06

    Syera Space Astronaut LED Finger Lights Recalled Due to Battery Ingestion Risk

    Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.

    Product
    Space Astronaut LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V510000·2026-08-06

    Alfa Romeo Tonale and Dodge Hornet vehicles recalled for seat belt failure

    Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.

    Product
    ALFA ROMEO — ALFA ROMEO, DODGE TONALE, HORNET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V514000·2026-08-06

    Toyota 2024 Tacoma rear shock absorber suspension recall issued

    Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.

    Product
    TOYOTA — TOYOTA TACOMA HYBRID, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V515000·2026-08-06

    Mack Recalls 2027 Anthem and Pioneer Trucks for Marker Light Defect

    Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.

    Product
    MACK — MACK ANTHEM AN (4), PIONEER PR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1189-2026·2026-08-05

    Requeson Soft Ricotta Recalled Due to Possible Listeria Contamination

    Nelson & Isa Lacteos LLC is recalling 480 1-lb packages of Requeson soft ricotta sold in NY because the product may be contaminated with Listeria monocytogenes.

    Product
    Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2735-2026·2026-08-05

    ResMed Astral 100/150 Ventilators Recalled Due to Electrolyte Leakage Risk

    ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.

    Product
    Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2792-2026·2026-08-05

    Cardiovascular Procedure Kits Recalled Due to Particulate in Fluid Path

    Medical Action Industries is recalling cardiovascular procedure kits containing manifolds that may have particulate in the fluid path, which could enter blood circulation and lodge in blood vessels. FDA Class I.

    Product
    Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
    Category
    Medical Device
    Distribution
    2 states
  • 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-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
  • 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
  • HighFDA (Devices)·Z-2799-2026·2026-08-05

    Medical Convenience Kits Recalled Over Endotoxin Variability in Neurological Sponges

    Windstone Medical Packaging is recalling 465 AMS medical convenience kits in connection with a Medicom recall of Ritmed Neurological Sponges due to potential endotoxin level variability.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack, Part Number AMS10411C; 3) Rhinoplasty Pack, Part Number AMS11963A; 4) Spine Pack, Part Number AMS12636C; 5) Lumbar Lami Pack, Part Number AMS12731; 6)…
    Category
    Medical Device
    Distribution
    Distributed nationwide