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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19126–19150 of 39605

  • SevereFDA (Food)·F-0489-2018·2017-12-20

    Wang Globalnet Recalls Fish Balls for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Ball in Polybag 24/12oz. because the product contains undeclared egg and wheat.

    Product
    Fish Ball in Polybag 24/12oz., Item no. 20072, UPC Code 087703200722
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0186-2018·2017-12-20

    Physio-Control Recalls Defibrillation Electrodes Due to Incorrect Pad Placement Artwork

    Physio-Control is recalling 14,219 LIFEPAK defibrillation electrodes because the artwork instructs incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0488-2018·2017-12-20

    Wang Globalnet Fish Cake Recalled for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Cake in Polybag due to undeclared egg and wheat ingredients. The product was distributed to several Northeastern and Mid-Atlantic states.

    Product
    Fish Cake in Polybag 20/1lb., Item no. 13125 UPC Code 087703131256
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0492-2018·2017-12-20

    Wang Globalnet Fish Cake Recalled for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Cake in Polybag 10/930g because it contains undeclared egg and wheat allergens.

    Product
    Fish Cake in Polybag 10/930g, Item no. 15731 UPC Code 087703157316
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0187-2018·2017-12-20

    Physio-Control Recalls LIFEPAK Electrode Starter Kits Due to Labeling Errors

    Physio-Control is recalling 14,219 LIFEPAK Electrode Starter Kits because the infant artwork shows incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V821000·2017-12-20

    FCA Recalls Ram Trucks Due to Transmission Shift Interlock Defect

    FCA is recalling specific Ram trucks because the brake transmission shift interlock pin may stick, allowing the vehicle to shift out of park without the brake pedal or key, increasing rollaway risk.

    Product
    RAM — RAM, DODGE 2500, 4500, 3500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0252-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment Risk

    Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.

    Product
    Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ Nit GW, UPN H965458950, Catalog No. 45-895 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V836000·2017-12-20

    Mobility Ventures Recalls MV-1 Vehicles for Seat Track Defect

    Mobility Ventures is recalling 2011-2016 MV-1 vehicles because the driver's seat may disengage from the track during a rear impact, increasing injury risk.

    Product
    MOBILITY VENTURES — MOBILITY VENTURES MV-1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0490-2018·2017-12-20

    Wang Globalnet Recalls Fish Tofu for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Tofu in Polybag 40/240g because the product contains undeclared egg and wheat allergens.

    Product
    Fish Tofu in Polybag 40/240g, Item no. 17185, UPC Code 087703171855
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0241-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included Greatbatch introducer sheaths have handles that may detach during use.

    Product
    XCELA PASV 5F DL 55CM IR-145 Nitinol Wire KIT PG, UPN H965251260, Catalog No. 25-126 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0242-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.

    Product
    XCELA PASV 5F DL 55CM MST-70 KIT PG, UPN H965457320, Catalog No. 45-732 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0491-2018·2017-12-20

    Wang Globalnet Fish Cake Recalled for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Cake in Polybag due to undeclared egg and wheat allergens. The product was distributed across 11 states.

    Product
    Fish Cake in Polybag 10/2.2lbs, Item no. 12842 UPC Code 087703128422
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0244-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.

    Product
    Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, UPN H965458180, Catalog No. 45-818 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V830000·2017-12-19

    Newmar Recalls 2016-2018 Motorhomes for Electrical Fire Risk

    Newmar is recalling 2,915 model year 2016-2018 motorhomes because a loose power connection at the Automatic Transfer Switch may cause heat buildup and increase the risk of a fire.

    Product
    NEWMAR — NEWMAR KING AIRE, BAY STAR, MOUNTAIN AIRE, CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V825000·2017-12-19

    2018 Coachmen Galleria Motorhomes Recalled for Wiring Fire Risk

    Forest River is recalling 2018 Coachmen Galleria motorhomes because an inverter lead wire may melt, increasing the risk of a fire.

    Product
    COACHMEN — COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V829000·2017-12-19

    REV Recalls 2018 Motorhomes Due to Electrical Wiring Short Risk

    REV Recreation Group is recalling 347 specific 2018 motorhomes because water may enter 12-volt harness connectors, potentially causing an electrical short and increasing the risk of a crash.

    Product
    MONACO — MONACO, AMERICAN COACH, HOLIDAY RAMBLER MARQUIS, AMERICAN REVOLUTION, AMERICAN DREAM, ENDEAVOR XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·129-2017·2017-12-16

    Piller's Fine Foods Recalls Ready-to-Eat Salami and Speck Due to Salmonella

    Piller's Fine Foods is recalling approximately 1,076 pounds of ready-to-eat salami and speck products due to possible Salmonella contamination. The products were distributed in five U.S. states.

    Product
    Piller's Fine Foods Recalls Ready-To-Eat Salami and Speck Products due to Possible Salmonella Adulteration
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V812000·2017-12-15

    Ducati Recalls Motorcycles Due to Front Brake Master Cylinder Failure Risk

    Ducati is recalling specific 2015-2018 motorcycles because front brake master cylinders may fail, increasing crash risk. Dealers will replace the piston free of charge.

    Product
    DUCATI — DUCATI MULTISTRADA, MONSTER 1200, 1299, SCRAMBLER 800 CAFE RACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V802000·2017-12-14

    REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Satellite Dish Defect

    REV Recreation Group is recalling 87 specific 2018 Fleetwood and Holiday Rambler motorhomes because the satellite dish may detach from the roof while driving, creating a road hazard.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER PACE ARROW, NAVIGATOR, BOUNDER, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V806000·2017-12-14

    Mazda Recalls 2004-2006 B-Series Trucks for Air Bag Inflator Defect

    Mazda is recalling 2004-2006 B-Series trucks because the passenger air bag inflator may rupture during deployment, sending metal fragments into the vehicle.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17T019000·2017-12-14

    Cooper Tires Recalled for Belt Separation Risk

    Cooper Tire & Rubber Co. is recalling specific tire models due to an incorrect belt rubber compound that may cause belt separation and loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18706·2017-12-14

    Crate and Barrel Recalls Dakota Benches Due to Fall Hazard

    Crate and Barrel is recalling Dakota wooden benches because they can tip over, posing a fall hazard. The company has received reports of injuries including broken bones and an amputation.

    Product
    Crate and Barrel Dakota benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0102-2018·2017-12-13

    Pravastatin Tablets Recalled Due to Incorrect Bupropion Filling

    International Laboratories is recalling Pravastatin Sodium Tablets 40 mg because they were filled with Bupropion hydrochloride XL Tablets 300 mg.

    Product
    Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16
    Category
    Drug
    Distribution
    Distributed nationwide