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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Minimum severity

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

Clear filters

8901–8925 of 36629

  • SevereFDA (Drugs)·D-0117-2022·2021-11-17

    Hydroxocobalamin Injection Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Hydroxocobalamin 1,000 MCG/mL injectable vials due to lack of assurance of sterility. The affected lot was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    HYDROXOCOBALAMIN 1,000MCG/ML INJ VIAL 1,000MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0186-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable Recalled Due to Sterility Assurance Failure

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.25/PGE-1 6 injectable vials due to lack of assurance of sterility. The injectable medication was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.25/PGE-1 6 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0143-2022·2021-11-17

    Sermorelin Acetate/Ipamorelin Vials Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Sermorelin Acetate 15MG/Ipamorelin 15MG lyophilized vials due to lack of assurance of sterility. The affected lot was distributed across the United States, Washington, D.C., and Puerto Rico.

    Product
    SERMORELIN ACETATE 15MG/IPAMORELIN 15MG - LYOPHILIZED 15MG/15MG VIAL, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·21V886000·2021-11-16

    Jayco Recalls 2020-2022 Motorhomes Due to Rear Suspension Fastener Defect

    Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA, REATTA XL, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·044-2021·2021-11-15

    Shamrock Foods Recalls Raw Ground Beef Patties Due to Plastic Contamination

    Shamrock Foods is recalling approximately 6,876 pounds of raw ground beef patties because they may contain pieces of hard, white plastic.

    Product
    Shamrock Foods Company — Shamrock Foods Company DBA Gold Canyon Meat Company Recalls Raw Ground Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V881000·2021-11-12

    Volvo Recalls 2021 XC40 BEV Vehicles Due to Loose Engine Bolt

    Volvo is recalling 2021 XC40 BEV vehicles because a bolt securing the electrical motor bracket may be loose or missing, which could reduce structural protection in a crash.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E094000·2021-11-12

    Chrysler Recalls Mopar High Pressure Fuel Pumps and 6.7L Engines

    Chrysler is recalling specific Mopar High Pressure Fuel Pumps and 6.7L Cummins Turbo Diesel Engines because the pump may fail, causing the engine to stall without warning.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V876000·2021-11-12

    2021-2022 Continental Cargo and Cargo Mate Trailers: Welding Defect in Coupler

    Forest River is recalling certain 2021-2022 Continental and Cargo Mate cargo trailers due to an improperly welded coupler. The defect may cause the trailer to separate from the tow vehicle, increasing crash risk.

    Product
    CARGO MATE — CARGO MATE, CONTINENTAL CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V878000·2021-11-12

    Alfa Romeo Stelvio and Giulia fuel line sensor housing cracks

    The fuel line sensor housing in certain 2020-2021 Alfa Romeo Stelvio and Giulia vehicles may crack and leak fuel, causing engine stalls and increasing fire risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V880000·2021-11-12

    Chrysler Recalls 2019-2020 Ram Trucks for Fuel Pump Failure Risk

    Chrysler is recalling 2019-2020 Ram trucks with Cummins 6.7L diesel engines because the high-pressure fuel pump may fail, causing sudden engine stalls that increase crash risk.

    Product
    RAM — RAM 5500, 3500, 4500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V882000·2021-11-12

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc and increasing fire risk.

    Product
    WESTERN STAR — WESTERN STAR 5700, 4900, 4700, 6900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·042-2021·2021-11-10

    Citterio Salame Sticks Recalled for Possible Salmonella Contamination

    Euro Foods is recalling Citterio salame sticks due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Euro Food, Inc., DBA Citterio USA Corporation — Euro Foods Dba Citterio USA Corp. Recalls Salame Stick Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0087-2022·2021-11-10

    Irbesartan Tablets Recalled for Impurity in Active Ingredient

    Lupin Pharmaceuticals is recalling Irbesartan tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects 30-count and 90-count bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V872000·2021-11-10

    Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak

    Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE, LEVANTE, MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0090-2022·2021-11-10

    Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0158-2022·2021-11-10

    Seafood Products Recalled for Salmonella Contamination Risk

    Northeast Seafood Products is recalling multiple seafood products including haddock, salmon, and trout due to potential Salmonella contamination. The products were distributed to restaurants and grocery stores in Colorado between May and October 2021.

    Product
    Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod, Halibut, Coho Salmon, Atlantic Salmon Portions, Lane Snapper, Tilapia, All Natural Salmon Fillet, Pacific Sole, and Farm Raised Striped Bass
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V873000·2021-11-10

    Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect

    The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2022·2021-11-10

    Cubicin daptomycin injection recalled for glass particle contamination

    Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.

    Product
    Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0114-2022·2021-11-10

    Green Giant Fresh Whole Yellow Onions Recalled for Salmonella Risk

    POTANDON PRODUCE LLC is recalling Green Giant Fresh whole yellow onions sold in 2 lb., 3 lb., and 5 lb. bags due to potential Salmonella Oranienburg contamination. The product was distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green Giant Fresh whole YELLOW onions in 3 lbs. flexible mesh bags, (16/3 lb. pkg. per case) - UPC 60580600123-9. Green Giant Fresh whole YELLOW onions in 5 lbs. fl
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0194-2022·2021-11-10

    IPL Coupling Gel and EcoGel 200 Recalled for Bacterial Contamination

    Lumenis, Inc. is recalling IPL Coupling Gel and EcoGel 200 due to potential bacterial contamination. Approximately 11,064 units were distributed worldwide.

    Product
    IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL Coupling Gel or EcoGel 200, 0.25 L (AX1009012) manufactured by Eco-Med Pharmaceutical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0111-2022·2021-11-10

    Raw Red Onions Recalled Due to Salmonella Oranienburg Risk

    ProSource Produce LLC has recalled whole raw red onions imported from Chihuahua, Mexico, due to potential Salmonella Oranienburg contamination. The affected product was distributed across multiple U.S. states and Canadian provinces.

    Product
    Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Markon
    Category
    Food
    Distribution
    36 states