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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26551–26575 of 114586

  • ModerateFDA (Devices)·Z-0736-2023·2022-12-28

    Bone Cement Recall: Missing Turkish Language Instructions for Use

    Howmedica Osteonics Corp. is recalling Full Dose CE Simplex P Single Bone Cement because the included instructions for use lack Turkish language translations. The product content itself is accurate; only the language translation is missing.

    Product
    Full Dose CE Simplex P Single Bone Cement - Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number: 6191-0-001
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0725-2023·2022-12-28

    Intradental periodontal picks recalled for mislabeling by Young Dental

    Young Dental Manufacturing has recalled Denticator PICK-A-DENT intradental picks due to mislabeling. The recall affects 600 packs distributed in Iowa, New York, Pennsylvania, Tennessee, Texas, and Canada.

    Product
    Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0729-2023·2022-12-28

    GE Patient Monitors May Display Inaccurate CO2 Readings at Non-Sea-Level Locations

    GE Healthcare is recalling certain B105P patient monitors because they may display inaccurate CO2 measurements when used in locations not at or near sea level with mmHg or kPa units selected.

    Product
    B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0202-2023·2022-12-28

    Take 2 frozen pizza dough recall due to packaging debris contamination

    It'll Be Pizza is recalling Take 2 frozen pizza dough products (1,678 cases) distributed across Maine, Vermont, Massachusetts, Pennsylvania, and New Hampshire due to possible contamination with foreign debris from packaging.

    Product
    Take 2 Classic 18 oz, 24 ct/case; Take 2 Classic 20 oz, 22 ct/case; Take 2 Specialty Traditional 20oz, 22ct/case frozen pizza dough manufactured by It'll Be Pizza
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·22V955000·2022-12-23

    Mercedes-Benz Recalls GLE and ML Models for Fuel Pump Water Damage

    Mercedes-Benz is recalling 2012-2020 GLE and ML models because water in the spare tire well can damage the fuel pump control unit, causing engine stalls.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML350, ML550, ML250, AMG ML63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V954000·2022-12-23

    Mercedes-Benz Recalls Vehicles Due to Sunroof Panel Detachment Risk

    Mercedes-Benz is recalling 2001-2011 C, CLK, E, and CLS class vehicles because the glass sunroof panel may detach, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ AMG E63, CLK500, CLS550, E550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V953000·2022-12-23

    2020-2023 Lincoln Aviator and Corsair Seat Belt Warning Chime Duration Defect

    Ford is recalling certain 2020-2023 Lincoln Aviators and Corsairs because the seat belt warning chime may activate for less than 4 seconds, failing to properly alert unbelted drivers.

    Product
    LINCOLN — LINCOLN AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E101000·2022-12-23

    Warn Industries Recalls Winch Remotes Due to Water Intrusion Risk

    Warn Industries is recalling wireless winch remotes because water intrusion can cause corrosion, leading to unintentional winch operation and injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23078·2022-12-22

    Target Recalls Pillowfort Weighted Blankets Due to Asphyxiation Risk

    Target is recalling about 204,000 Pillowfort Weighted Blankets because children can become entrapped inside the blanket cover, creating a risk of asphyxiation. Two children have died from this hazard.

    Product
    Pillowfort™ Weighted Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·045-2022·2022-12-22

    Morasch Meats Recalls Raw Frozen Diced Beef Due to E. Coli O157:H7

    Morasch Meats is recalling approximately 3,930 pounds of raw frozen diced beef products produced on August 24, 2022, due to possible E. coli O157:H7 contamination.

    Product
    Morasch Meats, Inc — Morasch Meats Inc. Recalls Raw Frozen Diced Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23080·2022-12-22

    Samsung Top-Load Washing Machines Recalled for Fire Hazard

    Samsung has recalled about 663,500 top-load washing machines because the machines can short-circuit and overheat, posing a fire hazard. A free software update is available to resolve the issue.

    Product
    Samsung Top-Load Washing Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V951000·2022-12-22

    Motorhomes recalled for faulty LPG service valves causing propane leak risk

    Kibbi is recalling 2022–2023 Renegade Valencia motorhomes. Service valves on LPG tanks may be improperly connected, creating a propane leak risk that could lead to fire if an ignition source is present.

    Product
    RENEGADE — RENEGADE, RENEGADE RV VALENCIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V950000·2022-12-22

    2022 Acura TLX Tire Damage Recall Due to Bead Cuts and Tears

    Honda is recalling approximately 19 model-year 2022 Acura TLX vehicles because their tires may have sustained cuts and tears. Damaged tires can lead to loss of vehicle control and increase crash risk.

    Product
    ACURA — ACURA TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23075·2022-12-22

    GASGAS Off-Road Motorcycles Recalled for Engine Failure and Crash Hazards

    KTM North America is recalling about 231 GASGAS MC 250 motorcycles due to an incorrectly programmed CDI box that can cause engine failure and pose crash and injury hazards. Consumers should stop riding the motorcycles immediately and contact an authorized dealer for a free repair.

    Product
    GASGAS Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23077·2022-12-22

    Pacific 20-Inch Kids' Bicycles Recalled for Loose Handlebar Fall Hazard

    Pacific Cycle is recalling about 147,000 Pacific Igniter and Pacific Bubble Pop 20-inch bicycles sold at Target because the handlebars can become loose during use, posing a fall hazard. Ten injuries involving bruising and abrasions have been reported.

    Product
    Pacific Igniter and Pacific Bubble Pop 20" kids' bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23076·2022-12-22

    BLU3 Nomad Battery-Powered Tankless Diving Systems Recalled for Drowning Hazard

    BLU3 is recalling about 1,300 Nomad battery-powered tankless diving systems because the compressor head can fracture during use, restricting airflow and posing a drowning hazard to divers. No injuries have been reported.

    Product
    Nomad Battery-Powered Tankless Diving Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V948000·2022-12-22

    Shadow Living Quarter Travel Trailers Recalled for Gas Leak Risk

    Shadow Trailer is recalling 2021-2022 Living Quarter travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    SHADOW — SHADOW LIVING QUARTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V949000·2022-12-22

    2021-2023 Holiday Rambler and Fleetwood Motorhomes: Propane Tank Valve Defect

    REV Recreation Group is recalling certain 2021-2023 Holiday Rambler and Fleetwood motorhomes due to service valve defects on LPG tanks that may cause propane leaks and fire risk. Dealers will replace valves at no cost.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, BOUNDER, SOUTHWIND, FORTIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V947000·2022-12-22

    2022 RAM PROMASTER recalled for inoperative rearview camera

    Chrysler recalls 2022 RAM PROMASTER vehicles with an incorrect rearview camera that cannot be installed, reducing rear visibility and increasing crash risk.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23081·2022-12-22

    Nova Medical Home Bed Rails Recalled Due to Entrapment and Asphyxia Risk

    Nova Medical Products is recalling approximately 20,000 Home Bed Rails (Models 6093 and 6094) because users can become entrapped within the bed rail or between the rail and mattress, posing a serious risk of death by asphyxiation.

    Product
    Home Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0438-2023·2022-12-21

    Arrow AC3 Optimus IABP recalled for shortened battery run-times

    Arrow AC3 Optimus Intra-Aortic Balloon Pump (IABP) devices are recalled worldwide due to a potential issue with shortened battery run-times. All lot and serial numbers of model IAP-0700 are affected.

    Product
    Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700 (IPN001112), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0436-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Battery Runtime Issue

    Arrow International is recalling the AutoCAT2 Intra-Aortic Balloon Pump due to a potential issue with short battery run-times. All lot and serial numbers worldwide are affected.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN916548), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0434-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Battery Run-Time Issue

    ARROW INTERNATIONAL is recalling Arrow AutoCAT2 Intra-Aortic Balloon Pumps due to a potential issue with short battery run-times. Affected devices distributed worldwide may have reduced battery endurance.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN917287), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0428-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Recalled for Short Battery Run-Times

    Arrow AutoCAT2 intra-aortic balloon pumps are being recalled due to a potential issue with short battery run-times. The recall affects 12 units distributed worldwide.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2, REF IAP-0435 (IPN000312), cardiac pump
    Category
    Medical Device
    Distribution
    0 states