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.

Filters

Agency

Category

Minimum severity

Clear filters

37176–37200 of 39777

  • SevereFDA (Drugs)·D-1425-2012·2012-08-01

    Grandpa Brands Recalls Dent's Extra Strength Toothache Gum

    Grandpa Brands Co is recalling Dent's Extra Strength Toothache Gum due to superpotent benzocaine levels. Consumers should stop using the product.

    Product
    Dent's Extra Strength Toothache Gum, (benzocaine 20%), Net Wt. .035 Oz.. (1 g) box, C.S. Dent & Co., Erlanger, KY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2040-2012·2012-08-01

    GE OEC 6800 Miniview X-ray System Recalled for Safety Issues

    GE OEC Medical Systems is recalling 1,933 OEC 6800 Miniview fluoroscopic x-ray systems due to intermittent safety issues, including navigation tracking inaccuracy and system lock-ups.

    Product
    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1774-2012·2012-08-01

    Cass Clay Creamery Recalls Peppermint Ice Cream for Undeclared Eggs

    Cass Clay Creamery is recalling Peppermint Bon Bon Light Ice Cream in Minnesota, Wisconsin, North Dakota, and Iowa because the products contain undeclared eggs.

    Product
    Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 41130-21663, Distributed by Supervalu Inc, Eden Prairie, MN 55344. SunnyBrook, Peppermint Bon Bon Light Ice Cream, Half…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1791-2012·2012-08-01

    East Bay Seafood Recalls Frozen Yellow Fin Tuna Loins for Histamine Levels

    East Bay Seafood Co., Inc. is recalling 30,360 pounds of frozen yellow fin tuna loins imported from Vietnam because testing revealed histamine levels over 50 ppm.

    Product
    Frozen Yellow Fin Tuna Loins (AAA)Co Treated Skinless Frozen. 44 lbs./carton (3-4 Loins/Case) Imported from Vietnam
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1783-2012·2012-08-01

    Arctic Zero Frozen Dessert Bars Recalled for Undeclared Milk

    Arctic Zero, Inc. is recalling specific frozen dessert bars due to undeclared milk, a major allergen.

    Product
    Chocolate Dipped Bars 2 Strawberry and 2 Orange Cream, 2.1 Fl oz bars, UPC 8 52244 00309 1
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1775-2012·2012-08-01

    Arctic Zero Frozen Dessert Recalled for Undeclared Milk

    Arctic Zero, Inc. is recalling its frozen dessert products due to undeclared milk, a major food allergen.

    Product
    Chocolate, 1pt., UPC 8 52244 00300 8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1779-2012·2012-08-01

    Arctic Zero Frozen Dessert Recalled for Undeclared Milk

    Arctic Zero, Inc. is recalling its frozen dessert products, including Chocolate Peanut Butter, due to undeclared milk.

    Product
    Chocolate Peanut Butter, 1pt., UPC 8 52244 00301 5
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1805-2012·2012-08-01

    Hanmi Recalls Frozen Oysters Due to Potential Norovirus Contamination

    Hanmi Incorporated is recalling specific lots of Surasang brand frozen oysters because they may have been exposed to human fecal waste and are potentially contaminated with norovirus.

    Product
    Frozen Oyster, IQF, Surasang Brand, 1) 8 oz, packed in plastic bags, 40 bags/case, Item No.: 03777; 2) 2.5 lb, packed in plastic bags, 10 bags/case, Item No.: 06413.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1793-2012·2012-08-01

    Pacific American Fish Recalls Korean Oysters Due to Insanitary Conditions

    Pacific American Fish Co Inc is recalling specific lots of Korean Oysters because they were prepared under insanitary conditions, posing a potential health risk.

    Product
    Oyster Half Shell Farm, OYS107, 144ps/cs, Oyster Half Shell small Farm, OYS114, 144ps/cs,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1784-2012·2012-08-01

    Arctic Zero Frozen Dessert Bars Recalled for Undeclared Milk

    Arctic Zero, Inc. is recalling specific frozen dessert bars because they contain undeclared milk, a major food allergen.

    Product
    Chocolate Dipped Bars, 2 Chocolate & 2 Vanilla, 2.1 fl oz bars, UPC 8 52244 00308 4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2082-2012·2012-08-01

    Hill-Rom Recalls Affinity Four Birthing Beds Due to Fall Risk

    Hill-Rom is recalling 12,726 Affinity Four Birthing Beds because bed movement during labor may cause patient or caregiver falls.

    Product
    Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery ) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1772·2012-08-01

    Eden Apple Juice Recalled Due to Arsenic Levels

    S. Bertram Inc. is recalling Eden Quality Product Pasteurized Apple Juice because laboratory tests found arsenic at 36.4 parts per billion.

    Product
    Eden Quality Product Pasteurized Apple Juice from concentrate vitamin C added in a 46 fluid ounce can. Service Size 8 fl oz. Dist. by S. Bertram Inc., Linden, NJ 07036. Concentrate from China.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1796-2012·2012-08-01

    B & F, Inc. Recalls Frozen Oysters Due to Insanitary Conditions

    B & F, Inc. is recalling Z.Shell Sanggul and Z.Shell HS frozen oysters because they were prepared or held under insanitary conditions, posing a potential health risk.

    Product
    Frozen Oysters are packaged in 8 oz. 40 oz, and 3 lbs. The item numbers are 06413, 03777, FO/HS-OT8; 136300-20110430. The brand names are Z.Shell Sanggul and Z.Shell HS.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2076-2012·2012-08-01

    CareFusion Alaris PC Unit Model 8015 Recalled for Power Supply Board Error

    CareFusion 303, Inc. is recalling Alaris PC unit model 8015 devices because a power supply board component causes startup error codes and alarms.

    Product
    Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2077-2012·2012-08-01

    Anspach Effort Recalls Sterile Bone Cutting Burrs Due to Breakage Risk

    The Anspach Effort, Inc. is recalling specific sterile bone cutting burrs because the cutter may come apart during use.

    Product
    .***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2038-2012·2012-08-01

    GE OEC 9800 C-arm Systems Recalled for Power Supply Defect

    GE OEC Medical Systems is recalling 8,214 OEC 9800 C-arm systems worldwide because the vertical lift column power supply is defective and subject to early life failure.

    Product
    OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional…
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·12V371000·2012-07-31

    Newmar Grand Star Motorhomes Recalled for Brake Performance Issues

    Newmar is recalling 2008-2009 Grand Star Class A motorhomes because brake caliper pistons may grow, causing drag and reduced braking performance.

    Product
    NEWMAR — NEWMAR GRAND STAR CA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V365000·2012-07-31

    Dutchmen Recalls 2013 Coleman Travel Trailers Due to Propane Line Defect

    Dutchmen is recalling 2013 Coleman and Dutchmen travel trailers because the propane line may be damaged by the rear axle, posing a fire or explosion risk.

    Product
    COLEMAN — COLEMAN, DUTCHMEN TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V370000·2012-07-31

    Cottrell Recalls 2006-2011 Trailers Due to Bearing Failure Risk

    Cottrell is recalling 2006-2011 trailers with Meritor axles because low bearing durability can cause wheel end fires. Owners should contact Meritor for free repairs.

    Product
    COTTRELL — COTTRELL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide