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 deaths or serious injuries are reported, 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.

Filters

Agency

Category

Minimum severity

Clear filters

1151–1175 of 36490

  • CriticalFDA (Devices)·Z-1147-2026·2026-01-28

    Full electric lightweight homecare beds recalled over pendants that may overheat

    Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-inv
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1012-2026·2026-01-28

    Semi electric lightweight homecare beds recalled over pendants that may overheat

    Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1014-2026·2026-01-28

    Full electric low homecare beds recalled over hand pendants that overheat

    Medline is recalling 22,565 units of the Full Electric Low Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1013-2026·2026-01-28

    Full electric basic homecare beds recalled over pendants that may overheat

    Medline is recalling 138,412 units of the Full Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1102-2026·2026-01-28

    Frozen cookie dough recalled over undeclared peanuts in white chocolate macadamia

    Gregory's Foods is recalling 308 cases of Bag Full of Cookies White Chocolate Macadamia Nut frozen cookie dough over undeclared peanuts.

    Product
    RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan 10B. Radiation Therapy Treatment Planning System
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1016-2026·2026-01-28

    Full electric low lightweight homecare beds recalled over overheating pendants

    Medline is recalling 15,581 units of the Full Electric Low Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
    Category
    Medical Device
    Distribution
    4 states
  • SevereNHTSA·26V050000·2026-01-28

    Ducati motorcycle rear brake hose may fail from excessive heat

    Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.

    Product
    DUCATI — DUCATI STREETFIGHTER V4, PANIGALE V4, STREETFIGHTER V4 S, PANIGALE V4 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V044000·2026-01-26

    Grand Design fifth wheel U-bolts may loosen and shift the axle

    Grand Design is recalling certain 2021-2024 Momentum and 2022-2024 Solitude fifth wheel trailers because the U-bolt may become loose, causing the axle to move out of position.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V037000·2026-01-23

    Polestar 3 rear seat backrest striker brackets may be loose

    Polestar is recalling certain 2025 Polestar 3 vehicles because the striker brackets that secure the rear seat backrest may be loose. This fails FMVSS 207.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V035000·2026-01-23

    FWMoto Recalls FLY-10 E-Bikes Due to Insufficient Brake Performance

    FWMoto is recalling 2022-2024 FLY-10 e-bikes because brake pads may provide insufficient braking performance, increasing the risk of a crash.

    Product
    FLY E-BIKE — FLY E-BIKE, FWMOTO FLY-10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V042000·2026-01-23

    Grand Design Lineage solar panel adhesive may fail allowing detachment

    Grand Design is recalling certain 2025-2026 Lineage recreational vehicles because the adhesive securing the solar panels to the roof may fail, allowing a panel to detach.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V040000·2026-01-23

    Forest River Bus Recalls 2026 Collins Buses for Body Panel Adhesive Defect

    Forest River Bus is recalling 2026 Collins Bus transit buses because body panel adhesive may be applied incorrectly, causing panels to separate and reducing structural integrity.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS COLLINS BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26215·2026-01-22

    Semi electric homecare beds recalled over hand pendants that may overheat

    Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Mikario Trading 5-in-1 Convertible Baby Gyms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·26204·2026-01-22

    Pull string teething toys recalled over silicone strings that can lodge

    About 6,800 Yetonamr Pull String Teething Toys are being recalled because the silicone strings can reach the back of the throat and become lodged. CPSC is aware of 32 choking incidents.

    Product
    Yetonamr Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V031000·2026-01-22

    Chevrolet Blazer EV parking brake may activate unintentionally or fail

    GM is recalling certain 2024-2025 Chevrolet Blazer EV vehicles that may have been repaired incorrectly under recall 25V433, because the rear parking brake wiring harness may become damaged or corroded.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1023-2026·2026-01-21

    Libre 3 Plus sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1052-2026·2026-01-21

    Holiday cookie tins recalled over undeclared almond, pecan and walnut

    One Roof LLC is recalling 197 Atwater's Holiday Cookie Tins over undeclared tree nut allergens: almonds, pecans and walnuts.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1020-2026·2026-01-21

    Glucose monitoring sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1022-2026·2026-01-21

    Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up

    Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Food)·H-0393-2026·2026-01-21

    Moringa powder recalled over possible contamination with Salmonella Richmond

    Organic Living Superfoods is recalling 88 lbs of Healthy Truth brand Moringa Powder because the products may be contaminated with Salmonella Richmond. The action is Class I.

    Product
    Healthy Truth brand Moringa Powder; 5lb and 20lb
    Category
    Food
    Distribution
    5 states