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.

Filters

Agency

Category

Minimum severity

Clear filters

7001–7025 of 7514

  • SevereFDA (Drugs)·D-0175-2022·2021-11-17

    Testosterone Cypionate Injectable Compounded Injection Lacks Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Testosterone Cypionate 200mg/Anastrozole 1.5mg/mL injectable due to lack of assurance of sterility. The product was distributed in the United States including Washington, D.C. and Puerto Rico.

    Product
    TESTOSTERONE CYPIONATE 200MG/ANASTROZOLE 1.5MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0190-2022·2021-11-17

    TRI-MIX Papaverine Injectable Recalled Due to Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 17.65/PHENTOLAMINE 0.59/PGE-1 5.9 injectable due to lack of assurance of sterility.

    Product
    TRI-MIX PAPAVERINE 17.65/PHENTOLAMINE 0.59/PGE-1 5.9 INJ **T 101** INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0205-2022·2021-11-17

    Tri-Mix Papaverine Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine 30/Phentolamine 1/PGE-1 2.5 injectable due to lack of assurance of sterility. The recall affects 30 vials distributed across the United States.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 2.5 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0176-2022·2021-11-17

    Testosterone Cypionate/Anastrozole Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling testosterone cypionate 200 mg/anastrozole 1.75 mg/mL injectable due to lack of assurance of sterility. The affected lot was distributed across the United States including Washington, D.C. and Puerto Rico.

    Product
    TESTOSTERONE CYPIONATE 200MG/ANASTROZOLE 1.75MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0201-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable from Talon Compounding Pharmacy Recalled

    Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 30 injectable medication due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 30 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0202-2022·2021-11-17

    Tri-Mix Injectable Lacks Sterility Assurance, Compounding Pharmacy Recall

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine/Phentolamine/PGE-1 injectable due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 40 /ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0207-2022·2021-11-17

    TRI-MIX Injectable Compounded Drug Recalled for Sterility Assurance Failure

    Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 injectable medication due to lack of assurance of sterility. The product was distributed across the United States, Washington, D.C., and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 INJ**T 106** INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0216-2022·2021-11-17

    Tri-Mix Papaverine Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine 30/Phentolamine 3/PGE-1 100 injectable due to lack of assurance of sterility. The affected lot was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 3/PGE-1 100 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0221-2022·2021-11-17

    Tri-Mix Papaverine Injectable Lacks Sterility Assurance

    Talon Compounding Pharmacy is recalling a lot of Tri-Mix Papaverine injectable due to lack of assurance of sterility. The recalled product is distributed across the United States.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 4/PGE-1 5 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    0 states
  • 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
    CONTINENTAL CARGO — 2021 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 — 2020 ALFA ROMEO STELVIO
    Category
    Vehicle
    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 (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 (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
    35 states
  • SevereFDA (Food)·F-0112-2022·2021-11-10

    Raw Yellow Onions from Mexico Recalled for Salmonella Oranienburg

    ProSource Produce LLC is recalling whole raw yellow onions imported from Chihuahua, Mexico, due to potential contamination with Salmonella Oranienburg. The affected onions were distributed across multiple U.S. states and Canadian provinces under various brand names.

    Product
    Whole raw YELLOW 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, Mark
    Category
    Food
    Distribution
    35 states
  • SevereFDA (Devices)·Z-0119-2022·2021-11-10

    Monoject Prefilled Syringe Plunger Defect Recall: Air Reintroduction Risk

    Monoject prefilled syringes in medical kits may have a plunger that rebounds after air expulsion, potentially reintroducing air into the syringe. This FDA Class I recall affects approximately 9,378 units distributed in Florida and Pennsylvania.

    Product
    Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical Solutions Custom Convenience Kits: AMS-9041CP Leaderflex Insertion Kit with Ultrasound, AMS-9046CP-1 Insertion Tray-RX, AMS8939A Universal Procedure Pack w/Sp
    Category
    Medical Device
    Distribution
    2 states
  • 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
    0 states
  • 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 — 2022 MASERATI MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0113-2022·2021-11-10

    ProSource Produce white onions recall for Salmonella contamination

    ProSource Produce LLC is recalling whole raw white onions imported from Mexico due to potential Salmonella Oranienburg contamination. The onions were distributed across 33 U.S. states and Canada.

    Product
    Whole raw WHITE 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, Marko
    Category
    Food
    Distribution
    35 states
  • SevereFDA (Food)·F-0094-2022·2021-11-10

    Chicken Flavor Food Additive Recalled for Salmonella Contamination

    Givaudan Flavours Corp is recalling a natural chicken rotisserie flavor product due to positive Salmonella detection. The affected batch was distributed to a single account in Indiana.

    Product
    AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg packages packaged in brown square boxes with blue plastic interior
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0115-2022·2021-11-10

    Green Giant Fresh White Onions Recalled for Salmonella Risk

    Green Giant Fresh whole white onions in 2 lb. mesh bags have been recalled due to potential Salmonella Oranienburg contamination. Affected products were distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg per case) - UPC 60580600218-2.
    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 (Drugs)·D-0089-2022·2021-11-10

    Irbesartan and Hydrochlorothiazide Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets 150/12.5 mg due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient, which resulted from CGMP deviations.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide