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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651–675 of 90233

  • SevereFDA (Devices)·Z-3057-2026·2026-09-09

    Medline Blood Culture Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1329-2026·2026-09-09

    Fayus Inc. Recalls OLA-OLA Pounded Yam for Undeclared Milk

    Fayus Inc. is voluntarily recalling OLA-OLA Pounded Yam (Iyan) IYANINSTANT in multiple sizes due to undeclared milk. The product was distributed in six US states and two foreign countries.

    Product
    OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDIENTS: Processed Dehydrated Yam Flour, freshness preserved by BHT & sodium bisulfite. UPCs: (2 lb): 650655244825, (4 lb): 650655496873, (5 lb): 650655244856…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0817-2026·2026-09-09

    Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to CGMP deviations. The affected product was distributed in the US, Puerto Rico, and Chile.

    Product
    CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1319-2026·2026-09-09

    Savor Seasonings Recalls Organic Cheddar Seasoning for Undeclared Milk Allergen

    Savor Seasonings LLC is recalling Organic Cheddar Type Seasoning because it tested positive for undeclared milk. The product was distributed to one consignee in Canada.

    Product
    Organic Cheddar Type Seasoning, NET WT: 50 lbs. Product is packaged in bulk poly-lined paper bag. Savor Seasonings, LLC. 4292 Armstrong Boulevard Batavia, OH 45103. Product distribution: 218 (50-lb) bags + 2 partial bags (27-lb and 34-lb, one from each lot respectively).
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·26V583000·2026-09-09

    Daimler Trucks Recalls Freightliner and Western Star Trucks for Brake Defect

    Daimler Trucks North America is recalling certain 2020-2023 Freightliner Cascadia and 2022 Western Star 49X trucks because corroded brake valves may cause the vehicle to pull during braking.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2026·2026-09-09

    El Eden Recalls Ineligible Pork Crackling Potato Chips from Colombia

    El Eden Import Distributor Corp. is recalling potato chips containing pork cracklings imported from Colombia because the country is ineligible to export meat to the U.S.

    Product
    El Eden Import Distributor Corp Recalls Ineligible Pork Cracklings Products Imported from The Republic of Colombia
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·H-1326-2026·2026-09-09

    Ukrop's Bread Pudding Recalled for Metal Fragments

    Ukrop's Homestyle Foods is recalling Bread Pudding with Vanilla Sauce due to the potential presence of metal fragments.

    Product
    Bread Pudding with Vanilla Sauce NET WT 13.8 OZ (39g) UPC 7 22515 28044 8 Ukrop's Homestyle Foods, LLC Richmond, VA 23230
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0820-2026·2026-09-09

    Baxter Recalls Vancomycin Injection Due to CGMP Deviations

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

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3060-2026·2026-09-09

    Medline C-Section Prep Kits Recalled for Potential Sterility Breach

    Medline is recalling 352 C-Section Prep kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) C-SECTION PREP, Model Number: DYNJ32702B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0814-2026·2026-09-09

    Baxter Recalls Nexterone Amiodarone Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Nexterone (amiodarone hydrochloride) injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    NEXTERONE — NEXTERONE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V578000·2026-09-09

    Ford Recalls 2023-2027 F-150 Trucks for Fuel Tank Securing Defect

    Ford is recalling 2023-2027 F-150 vehicles because the fuel tank may be improperly secured, posing risks of fuel leaks, engine stalls, or the tank detaching while driving.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • HighFDA (Devices)·Z-3040-2026·2026-09-09

    Philips Brilliance CT Systems Recalled for Unintended Radiation Issue

    Philips is recalling Brilliance CT systems due to an unintended radiation issue that could affect equipment performance.

    Product
    Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 728311.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-3046-2026·2026-09-09

    AVID Medical Recalls Halyard Neurological Sponges Due to Endotoxin Variability

    AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.

    Product
    Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01; 3) ANEURYSM PACK, Model/Item Number (kit) BPAY14-01; 4) SPINE PACK, Model/Item Number (kit) HSLM53-01…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1304-2026·2026-09-09

    Prince Italian Bread Recalled for Undeclared Sesame Allergen

    Prince Bakery Inc is recalling 150 units of Prince Italian Bread in New York because sesame is not declared in the ingredient statement.

    Product
    Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR, NIACIN, FERROUS SULFATE, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE SHORTENING (PARTIALLY HYDROGENATED…
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26V580000·2026-09-09

    Ford Recalls 2026 Bronco Vehicles Due to Air Bag Mounting Defect

    Ford is recalling 2026 Bronco vehicles because a metal burr on the side curtain air bag bracket may tear the bag during deployment, increasing injury risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0805-2026·2026-09-09

    Baxter Recalls Vancomycin Injection Due to Manufacturing Deviations

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

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3059-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.

    Product
    Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
    Category
    Medical Device
    Distribution
    Distributed nationwide