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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351–375 of 39703

  • SevereFDA (Devices)·Z-3053-2026·2026-09-09

    Medline Ultrasound Breast Pack Recalled for Potential Sterility Breach

    Medline is recalling 300 Ultrasound Breast Packs due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0808-2026·2026-09-09

    Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0834-2026·2026-09-09

    Teva Recalls Trazodone Hydrochloride Tablets Due to Foreign Material

    Teva Pharmaceuticals is recalling 175,392 bottles of Trazodone Hydrochloride 50 mg tablets because they may contain foreign tablets or capsules.

    Product
    TRAZODONE HYDROCHLORIDE — TRAZODONE HYDROCHLORIDE (TRAZODONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V582000·2026-09-09

    Ford Recalls 2023-2025 Mustang Mach E for Battery Software Defect

    Ford is recalling 2023-2025 Mustang Mach E vehicles with specific battery modules due to software errors that may cause power loss or fire.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3087-2026·2026-09-09

    Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk

    Fresenius Medical Care is recalling 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.

    Product
    5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0807-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling Daptomycin in Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50 mL (10 mg/mL), 500 mg total, in 50 mL Single Dose Container (24 bags/carton), Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0714-24.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-020-2026·2026-09-06

    Imported Pork Guanciale Recalled for Possible Listeria Contamination

    Prime Line Distributors and Ferrarini USA are recalling imported pork guanciale due to possible Listeria monocytogenes contamination found during routine testing.

    Product
    Prime Line Distributors, Inc. and Ferrarini USA, Inc. Recall Imported Ready-To-Eat Pork Guanciale Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    10 states
  • SevereCPSC·26746·2026-09-03

    Mondraker Recalls Mountain Bicycles with ONOFF S9 Carbon Handlebars

    Mondraker USA is recalling specific mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars because they may crack or fracture, posing a risk of serious injury or death.

    Product
    Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V573000·2026-09-03

    Nova Bus Recalls LFS Models Due to Coolant Sensor Defect

    Nova Bus is recalling 2022-2024 LFS and LFS Artic buses because a faulty coolant sensor may cause unexpected engine shutdowns, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26734·2026-09-03

    Amana Through-The-Wall Air Conditioners Recalled Due to Fire Risk

    Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.

    Product
    Amana Through the Wall (TTW) air conditioners or heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26731·2026-09-03

    CPSC Recalls Cambridge Audio Yoyo (M) Bluetooth Speakers Due to Fire Hazard

    Audio Partnership is recalling Cambridge Audio Yoyo (M) Bluetooth speakers because their lithium-ion batteries can overheat and cause fires. No injuries have been reported.

    Product
    Cambridge Audio Yoyo (M) Portable Bluetooth Speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1263-2026·2026-09-02

    FDA Recalls Addall XR Shot Liquid Dietary Supplement

    ZMB Enterprises is recalling Addall XR Shot liquid dietary supplements because they contain undeclared ingredients 1,4-DMAA, Phenylethylamine, and Phenibut.

    Product
    Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-1259-2026·2026-09-02

    FDA Recalls Glutinous Rice Balls with Undeclared Peanuts

    KHONG GUAN (HQ) is recalling Glutinous Rice Balls with Black Sesame Filling due to undeclared peanuts. The product was distributed in eight US states.

    Product
    Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-1262-2026·2026-09-02

    Sirna & Sons Jalapeno Peppers Recalled for Potential Salmonella Javiana

    Sirna & Sons Produce is recalling 249 bags of 1 lb jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed for food service use in Ohio and Pennsylvania.

    Product
    Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sirna & Sons Produce 7176 State Route 88, Ravenna, OH 44266, distributed for food service use only
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-1301-2026·2026-09-02

    Jaime's Foods ATX Recalls Jalapeno Ranch Due to Undeclared Egg Allergen

    Jaime's Foods ATX, LLC is recalling Jalapeno Ranch in 16 oz. glass jars because the product contains an undeclared egg allergen. The recall affects 102 cases distributed in Texas.

    Product
    Jalapeno Ranch, packed in 16 oz. glass jars, 6 jars per case, with UPC #199284564923.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-1264-2026·2026-09-02

    Outshine Strawberry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0803-2026·2026-09-02

    ACTHAR Gel Recalled for Presence of Glass and Stopper Particulate Matter

    Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2993-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Damage Risk

    Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.

    Product
    Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product Number/SKU 780-01KIT); 2) MEDLINE HUDSON RCI, CIRCUIT, NEO, DUAL LIMB HTD, COLUMN, Medline Product Number/SKU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1269-2026·2026-09-02

    Outshine Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars because they may contain glass pieces. Consumers should check for specific batch codes.

    Product
    Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0776-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1266-2026·2026-09-02

    Outshine Fruit Bars Grape Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.

    Product
    Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states