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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

526–550 of 90167

  • HighFDA (Devices)·Z-3118-2026·2026-09-16

    C.R. Bard Recalls SureStep Foley Trays Due to Wipe Contamination

    C.R. Bard is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A304400A UDI code: 00801741073847¿ 10801741073844 SureStep"…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3109-2026·2026-09-16

    AVID Medical Recalls Halyard IV Start Kits Due to Seal Defects

    AVID Medical is recalling 98 Halyard IV Start Kits because wrinkles in the paper lidding may breach the seal, compromising sterility assurance.

    Product
    Halyard IV Start Kit Non-Sterile REF: KRIV26-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3112-2026·2026-09-16

    Atrium Medical Recalls Getinge PVC Thoracic Catheters Due to Endotoxin Testing

    Atrium Medical is recalling specific lots of Getinge PVC Thoracic Catheters because one lot failed bacterial endotoxin testing.

    Product
    Getinge PVC Thoracic Catheter, Soft PVC Right Angle, 10 per Case; Size(Model Number): 1. 24FR(8124), 2. 28FR(8128), 3. 32FR(8132), 4. 36FR(8136);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3117-2026·2026-09-16

    C.R. Bard Recalls SureStep Catheter Trays Due to Wipe Contamination

    C.R. Bard is recalling SureStep Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300¿ 10801741183307 00801741183218¿ 10801741183215 00801741183232 10801741183239 00801741183225¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3114-2026·2026-09-16

    C.R. Bard Recalls Foley Catheter Trays Due to Wipe Contamination

    C.R. Bard is recalling 12,463 Foley and intermittent catheter trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00801741024825¿ 10801741024822 SureStep" Foley Tray System with Bardex¿ Lubricath Temp…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3119-2026·2026-09-16

    C.R. Bard Recalls SureStep Foley Trays Due to Wipe Contamination

    C.R. Bard Inc. is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.

    Product
    Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300316AC UDI-DI code: 00801741143250 SureStep" Foley Tray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3120-2026·2026-09-16

    HeartSine SAM Public Access Defibrillators Recalled for Damaged Membrane Tail

    HeartSine Technologies is recalling SAM 350P, 360P, and 450P defibrillators due to a damaged membrane tail that causes intermittent faults.

    Product
    HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with Gateway - 2 Min CPR UDI-DI code: 0506016712804 HeartSine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3113-2026·2026-09-16

    Atrium Medical Recalls Getinge PVC Thoracic Catheters Due to Endotoxin Testing

    Atrium Medical Corporation is recalling specific lots of Getinge PVC Thoracic Catheters because bacterial endotoxin testing results were out of specification.

    Product
    Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1335-2026·2026-09-16

    Prolon Everyday Apulian Almond & Cocoa Spread Recalled for Undeclared Tree Nuts

    L-Nutra Inc is recalling Prolon Everyday Apulian Almond & Cocoa Spread because it contains undeclared hazelnut, cashew, and pistachio.

    Product
    Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold screw on closure. UPC: 50040360530
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3134-2026·2026-09-16

    Nipro MedicaLyte Bicarbonate Powder Recalled for High Endotoxin Levels

    Nipro Renal Solutions is recalling MedicaLyte Bicarbonate Powder due to high endotoxin levels. The recall affects 2,327 cases distributed in the US, Guatemala, and Panama.

    Product
    MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3111-2026·2026-09-16

    Atrium Medical Recalls Getinge PVC Thoracic Catheters Due to Endotoxin Testing

    Atrium Medical Corporation is recalling specific lots of Getinge PVC Thoracic Catheters because an out-of-specification result was found in bacterial endotoxin testing.

    Product
    Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V595000·2026-09-14

    Grand Design Recalls 2026-2027 Lineage RVs Due to Tire Speed Rating Issue

    Grand Design is recalling 2026-2027 Lineage RVs with the optional 43 tire package because the vehicle's top speed may exceed the tire's rating, increasing crash risk.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V589000·2026-09-11

    Forest River Recalls 2024-2026 Rockport Trucks Due to Wiring Fire Risk

    Forest River is recalling 2024-2026 Rockport trucks because incorrectly routed wiring may contact the hood, causing a short circuit and increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V591000·2026-09-11

    Micro Bird Recalls G5e School Buses Due to Wiring Harness Routing Issue

    Micro Bird USA LLC is recalling 2025-2027 G5e school buses because a wiring harness may be incorrectly routed, potentially causing a loss of drive power and increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5e SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V593000·2026-09-11

    Micro Bird Recalls 2025-2026 G5e Transit Buses for Wiring Harness Defect

    Micro Bird is recalling 2025-2026 G5e transit buses because an incorrectly routed wiring harness may be damaged, causing a loss of drive power and increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5e TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V590000·2026-09-11

    Volkswagen Recalls 2018-2021 Models for Steering Rack Bolt Corrosion

    Volkswagen is recalling 2018-2021 Tiguan, Atlas, and Audi Q3 vehicles because a steering rack bolt may corrode and break, potentially causing loss of steering control.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI TIGUAN, Q3, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V594000·2026-09-11

    Micro Bird Recalls 2025-2026 G5e School Buses for Wiring Harness Defect

    Micro Bird is recalling 2025-2026 G5e school buses because an incorrectly routed wiring harness may be damaged by a metal bracket, causing a loss of drive power and increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5e SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V592000·2026-09-11

    Farber Specialty Recalls Vehicles with Defective Wheelchair Lift Controls

    Farber Specialty is recalling certain vehicles equipped with S-Series and K-Series wheelchair platform lifts because a failed electrical contactor may prevent the lift from stopping.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY FORD F650, FORD F600, WINNEBAGO WFJ33FS, FORD F550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26752·2026-09-10

    Sweet Cubby Recalls Children's Loungewear Sets Due to Burn Hazard

    Sweet Cubby is recalling children's loungewear sets that violate mandatory flammability standards, posing a risk of serious burn injuries or death.

    Product
    Sweet Cubby Children’s Loungewear Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26750·2026-09-10

    Junkins Recalls DHASUWT Hair Dryer Brushes Due to Electrocution and Fire Risks

    Junkins is recalling DHASUWT hair dryer brushes because they lack safety features, posing risks of electrocution, shock, and fire. Consumers should stop using the product and contact the company for a refund.

    Product
    DHASUWT Hair Dryer and Blow Dryer Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26756·2026-09-10

    AGA and La Cornue Dual Fuel Ranges Recalled for Fire and Explosion Risk

    AGA and La Cornue dual fuel ranges are recalled because a missing gas test port cap can cause gas leaks, posing a risk of fire or explosion.

    Product
    AGA Elise and Mercury Series Freestanding Dual Fuel Ranges and La Cornue CornuFé 90 and CornuFé 110 Series Freestanding Dual Fuel Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide