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.

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20926–20950 of 27455

  • HighFDA (Devices)·Z-0045-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Label

    Hobbs Medical is recalling Biliary Pigtail Stent Kits distributed from March 2018 to September 2020 due to incorrect expiration date labels that extend the shelf life beyond the actual safe period.

    Product
    Hobbs Biliary Pigtail Stent Kits Catalog Number: 6108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0015-2023·2022-10-19

    Hobbs Medical Polypectomy Snare recalled for incorrect expiration date on label

    Hobbs Medical is recalling its Polypectomy Snare for an incorrect expiration date on the label that extends shelf life. Affected devices were distributed in the US and other countries from March 2018 to September 2020.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 4563
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0010-2023·2022-10-19

    Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.

    Product
    Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0024-2023·2022-10-19

    Hobbs Posi-Stop Injection Needles Recalled for Incorrect Expiration Date Labeling

    Hobbs Medical, Inc. is recalling Posi-Stop Injection Needles with lot numbers ending in 'R' due to incorrect expiration dates on device labels. The mislabeling extends the apparent shelf life, potentially allowing use of expired sterile devices.

    Product
    Hobbs Posi-Stop Injection Needle Catalog Number: 4720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0075-2023·2022-10-19

    Tidal Seafood Yellowfin Tuna Saku Block Recalled for Elevated Histamine

    Tidal Seafood is recalling Yellowfin Tuna Saku Block products due to possible elevated histamine levels. The product was distributed to California, Texas, and New Mexico.

    Product
    Tidal Seafood Yellowfin Tuna Saku Block 10-15 oz Best Buy 6/17/2024
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0037-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration dates

    Hobbs Medical is recalling certain Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual validity. Affected devices distributed between March 2018 and September 2020 may be used beyond their true expiration date.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0016-2023·2022-10-19

    Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 4564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0017-2023·2022-10-19

    Hobbs Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling transbronchial aspiration needles with incorrect expiration dates on labels. The 18 affected units were distributed in the US, Canada, Austria, Belgium, Finland, and Norway from March 2018 to September 2020.

    Product
    Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0061-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates

    Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V781000·2022-10-18

    Harley-Davidson Touring and Trike Motorcycles Unintended Brake Light Illumination Recall

    Harley-Davidson is recalling certain 2019-2022 Touring, Trike, and CVO models due to a software error causing brake lights to illuminate without rider input. This malfunction may confuse other drivers and increase crash risk.

    Product
    HARLEY-DAVIDSON — 2021 HARLEY-DAVIDSON FLHTCUTGSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V779000·2022-10-17

    Peterbilt and Kenworth trucks recalled for digital display freeze

    PACCAR is recalling certain 2022-2023 Kenworth and Peterbilt trucks whose digital displays may freeze. A frozen display prevents critical safety information like vehicle speed and warning lights from appearing.

    Product
    PETERBILT — 2023 PETERBILT 367
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23006·2022-10-13

    U-Line Outdoor Freezers Recalled Due to Fire Hazard

    U-Line is recalling about 90 Outdoor Series 24-inch built-in convertible freezers that can overheat and pose a fire hazard. U-Line has received three reports of freezer fires with no injuries reported.

    Product
    U-Line Outdoor Series 24-inch Built-In Convertible Freezers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23702·2022-10-13

    Ski-Doo 2022 Snowmobiles Recalled Due to Fire Hazard

    BRP is recalling certain 2022 Ski-Doo snowmobiles with 850 E-TEC engines due to a loose fuel injector hose retainer screw that can cause fuel leaks and fires. The company has received five fuel-leak reports, resulting in two fires.

    Product
    Ski-Doo snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23007·2022-10-13

    Ancheer E-Bikes Recalled Due to Fire, Explosion and Burn Hazards

    About 22,000 Ancheer e-bikes with lithium-ion batteries are being recalled because the batteries can ignite, explode, or spark, causing fire and burn injuries. Consumers should stop using the recalled bikes immediately and contact Ancheer for a free replacement battery and mount.

    Product
    Ancheer E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23011·2022-10-13

    Children's Bathrobes Recalled for Flammability Standard Violation

    Ekouaer children's bathrobes fail to meet federal flammability standards for sleepwear, posing a burn risk to children. About 9,200 units sold on Amazon between March 2020 and July 2021 are affected.

    Product
    Children's Bathrobes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23009·2022-10-13

    Early Learning Centre Shape Sorter Toys Due to Choking Hazard

    Addo Play has recalled about 9,300 Early Learning Centre Little Senses Lights & Sounds Shape Sorter Toys sold on Amazon from October 2020 through August 2022. The red cube can detach during use and release a small white ball, posing a choking hazard to infants.

    Product
    Early Learning Centre Little Senses Lights & Sounds Shape Sorter Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23010·2022-10-13

    Children's Sleepwear Recalled for Flammability Standards Violation

    Jammers Apparel Group is recalling about 450 children's nightgowns sold at JCPenney from March to May 2022 because they fail to meet federal flammability standards and pose a burn risk to children.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23013·2022-10-13

    Cressi-Sub USA Recalls Scuba Buoyancy Compensator Devices for Drowning Hazard

    Cressi-Sub USA is recalling about 1,350 scuba buoyancy compensator devices (BCDs) with defective inflator hoses that may fail to inflate properly, posing a drowning hazard to divers.

    Product
    Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hose
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V767000·2022-10-13

    2022 Jeep Wrangler Fuel Pump Engine Stall Recall

    Chrysler is recalling 2020-2022 Jeep Wranglers, Gladiators, and Ram 1500s due to potential fuel pump failure that may cause engine stall, increasing crash risk. Dealers will replace the pump at no cost.

    Product
    JEEP — 2022 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23008·2022-10-13

    U.P. Fashion Children's Rings Recalled for Excess Lead Content

    U.P. Fashion is recalling approximately 1,800 children's rings sold nationwide at dollar stores and discount stores from April 2021 through July 2022 because the metal base contains lead levels exceeding the federal lead content ban.

    Product
    Children's Rings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V772000·2022-10-13

    2022 Nissan Titan XD Infotainment Reboot Disables Rearview Display

    Nissan is recalling certain 2022 Titan XD and related models because the in-vehicle infotainment system may continuously reboot when restarted, causing the rearview display to become inoperative and reducing rear visibility.

    Product
    NISSAN — 2022 NISSAN TITAN XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V766000·2022-10-13

    2022 RAM 1500 Front Seat Belt Retractors Recalled Due to Defect

    Certain 2022 RAM 1500 vehicles have front seat belt retractors with improperly welded components that may fail to restrain occupants during a crash. Chrysler is replacing the affected retractors free of charge.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V768000·2022-10-13

    Jeep Wrangler Plug-In Hybrid Battery Fuse Defect Increases Crash Risk

    Chrysler is recalling the 2022-2023 Jeep Wrangler PHEV for battery fuse defects caused by incorrect fasteners. The fuses can overheat and fail, causing loss of drive power and increasing the risk of a crash.

    Product
    JEEP — 2023 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0020-2023·2022-10-12

    Mushroom Stir Fry Blend recalled due to Listeria contamination

    Renaissance Food Group is recalling Mushroom Stir Fry Blend after testing detected Listeria monocytogenes in the finished product. Products were distributed to Alabama, Georgia, and South Carolina.

    Product
    Mushroom Stir Fry Blend, NET WT, 9 OZ (255g), Dist. By: Renaissance Food Group LLC 4322 Moreland Ave. Conley, GA 30288, UPC 8 26766 19110 2
    Category
    Food
    Distribution
    0 states