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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

35301–35325 of 39756

  • SevereFDA (Devices)·Z-0748-2013·2013-02-20

    GE Healthcare Recalls Infant Resuscitation Systems Due to Reversed Fittings

    GE Healthcare is recalling 276 Giraffe and Panda T-Piece Resuscitation Systems because oxygen and air inlet fittings were reversed during assembly.

    Product
    GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The T-piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag and Mask Resuscitation System provides the basic equipment required for pulmonary resuscitation of infants.
    Category
    Medical Device
    Distribution
    31 states
  • SevereFDA (Drugs)·D-161-2013·2013-02-20

    Lee Pharmaceuticals Recalls 12-Hour Sinus Nasal Spray Due to Microbial Contamination

    Lee Pharmaceuticals is recalling 12-Hour Sinus Nasal Spray products due to microbial contamination identified during testing.

    Product
    12-Hour Sinus (oxymetazoline hydrochloride) Nasal Spray, 0.05%, 1 FL OZ (30 mL), labeled as a) 12 HOUR SINUS Nasal Spray, Best Choice, Proudly Distributed By: Valu Merchandisers, Co., Kansas City, MO 64111, UPC 0 70038 61226 1; b) Nasal Spray Sinus, Distributed by Discount Drug…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0990-2013·2013-02-20

    Tropical Nut & Fruit Recalls Chia Seed Sticks for Undeclared Peanuts

    Tropical Nut & Fruit Co. is recalling 1,380 lbs of Chia ReCharged Stix Mix due to undeclared peanuts. The product was distributed in Florida and North Carolina.

    Product
    Labeled in part: "All Natural Chia ReCharged Stix Mix***Chia Seed Sticks***Net Wt. 5oz", UPC Code: 0 94184 01014 6
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0991-2013·2013-02-20

    Cheesy Broccoli Soup Recalled Due to Undeclared Shrimp

    Diversified Foods & Seasonings is recalling Cheesy Broccoli Soup because a consumer found shrimp in the product. The recall covers 189 cases distributed in Tennessee and Mississippi.

    Product
    CULINARY Creations (brand) CHEESY BROCCOLI SOUP, 3F3080, CONTAINS: 20/2 LB. CHUBS, NET WT. 40 LBS. 91816 KG), DIVERSIFIED FOODS AND SEASONINGS, INC, 1115 N. CAUSEWAY BLVD. STE.200, MANDEVILLE, LA 70471 1-800-835-3374, FOR INSTITUTIONAL USE ONLY, UPC 00732628330803
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·13V055000·2013-02-15

    Prevost Recalls H3-41 and H3-45 Coaches for Steering Defect

    Prevost is recalling 6,120 H3-41 and H3-45 coaches because a steering component may fracture, causing loss of vehicle control.

    Product
    PREVOST — PREVOST H3-41, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13725·2013-02-14

    John Deere Recalls Gator Utility Vehicles Due to Fire Hazard

    John Deere is recalling about 4,700 Gator RSX850i utility vehicles because oil filters may leak, posing a fire hazard. No injuries have been reported.

    Product
    Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-148-2013·2013-02-13

    Globe All Wellness Recalls Slim Xtreme Capsules Containing Unapproved Sibutramine

    Globe All Wellness is recalling Slim Xtreme Herbal Slimming Capsules because testing revealed the presence of sibutramine, an unapproved and withdrawn drug.

    Product
    SLIM XTREME Herbal Slimming Capsule, supplied in 30-count bottles. Another Product Forumulated and Distributed By: Globe All Wellness, LLC Hollywood, FL 33020 www.diet66.com Inquires Call 877.842.9873
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-157-2013·2013-02-13

    Bracco Recalls Isovue-370 Injection Syringes Due to Particulate Matter

    Bracco Diagnostic Inc. is recalling specific lots of Isovue-370 injection syringes because they contain particulate matter, including cellulose and polyvinyl fibers.

    Product
    Isovue -370 (Iopamidol) Injection 76%, Prefilled 10 x 75 mL (NDC 0270-1316-66), 10 x 100 mL (NDC 0270-1316-67), 10 x 125 mL (NDC 0270-1316-68) Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-154-2013·2013-02-13

    Hospira Recalls Carboplatin Injection Vials Due to Visible Crystals

    Hospira is recalling 31,326 vials of Carboplatin Injection due to visible crystals found during inspection. The product is distributed nationwide and in Puerto Rico.

    Product
    CARBOPLATIN — CARBOPLATIN (CARBOPLATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-147-2013·2013-02-13

    Mylan Recalls Lansoprazole Capsules Due to Foreign Topiramate Tablets

    Mylan Pharmaceuticals is recalling 1,894 bottles of lansoprazole 30 mg capsules because they may contain foreign topiramate 100 mg tablets.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-153-2013·2013-02-13

    Hospira Recalls Carboplatin Injection Vials Due to Crystallization

    Hospira Inc. is recalling 23,315 vials of Carboplatin Injection due to visible particulates identified as Carboplatin crystals.

    Product
    CARBOPLATIN — CARBOPLATIN (CARBOPLATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0777-2013·2013-02-13

    Winco Premier Lifecare Recliner 5400 Recalled for Fire Safety Non-Compliance

    Winco Mfg. is recalling 95 Premier Lifecare Recliner 5400 units because their foam and vinyl do not meet California's TB 133 fire protection standards.

    Product
    PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-158-2013·2013-02-13

    Bracco Recalls Isovue-300 Injection Syringes Due to Particulate Matter

    Bracco Diagnostic Inc. is recalling specific lots of Isovue-300 Injection syringes because they contain particulate matter identified as cellulose and polyvinyl fibers.

    Product
    Isovue -300 (Iopamidol) Injection 61% Prefilled, 10 x 100 mL Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany); NDC 0270-1315-67.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-155-2013·2013-02-13

    Zicam Nasal Spray Recalled for Burkholderia cepacia Contamination

    Matrixx Initiatives Inc is recalling Zicam Extreme Congestion Relief nasal spray due to potential contamination with Burkholderia cepacia. The recall covers 46,752 bottles distributed nationwide.

    Product
    Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel, 0.05%, 0.50 fl. oz. (15 mL) spray bottle, Developed and distributed by Zicam LLC, Scottsdale, Arizona 85255, a wholly owned subsidiary of Matrixx Initiatives Inc, NDC 62750-005-10, UPC 7 32216 20410 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V046000·2013-02-11

    Spartan Recalls Aerial Vehicles Due to Inclinometer Signal Failure

    Spartan is recalling 2005-2011 RMP 100 and 2008-2010 MMP 100 aerial vehicles because a faulty inclinometer may allow the platform to tilt dangerously, risking injury or property damage.

    Product
    SPARTAN — SPARTAN RMP 100, MMP 100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V042000·2013-02-08

    Fontaine Modified Navistar Trucks Recalled for Steering Assembly Defect

    Fontaine Modification is recalling 811 modified Navistar trucks because steering clips may come loose, potentially making the vehicle difficult to steer and increasing crash risk.

    Product
    FONTAINE — FONTAINE INT'L 7400 W/DUAL STEERIN, INT'L 4300 W/DUAL STEERIN, INT'L 4400 W/DUAL STEERIN, INT'L 7500 W/DUAL STEERIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V039000·2013-02-07

    Prevost Recalls Coaches Due to Throttle Control Software Defect

    Prevost is recalling specific model year 2008-2013 coaches equipped with Volvo engines because a software defect may cause the throttle to remain fixed at 1700 rpm, increasing crash risk.

    Product
    PREVOST — PREVOST XLII-45 ENTERTAINER, H3-45, X3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13117·2013-02-07

    BlueStar Residential Gas Wall Ovens Recalled for Fire Hazard

    Prizer Painter Stove Works is recalling about 940 BlueStar gas wall ovens due to a fire hazard caused by improper installation or damaged gas connectors.

    Product
    BlueStar™ residential gas wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V045000·2013-02-07

    BMW Recalls 2007-2010 X5 Vehicles Due to Brake Vacuum Pump Leak

    BMW is recalling 2007-2010 X5 SAVs with 8-cylinder engines because a brake vacuum pump leak may cause loss of power assist braking, increasing stopping distance.

    Product
    BMW — BMW X5 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13723·2013-02-07

    BRP Recalls Ski-Doo Snowmobiles Due to Fuel Leak Fire Hazard

    Bombardier Recreational Products is recalling about 10,200 Ski-Doo snowmobiles because a fuel pump fitting can break, causing a fuel leak and fire hazard.

    Product
    Ski-Doo® snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0964-2013·2013-02-06

    Dymatize Elite Fudge Brownie Protein Bar Recalled for Peanut Allergen

    Belmont Confections is recalling Dymatize Elite Gourmet Fudge Brownie protein bars because a consumer reported an allergic reaction to peanuts.

    Product
    DYMATIZE NUTRITION ELITE Gourmet Fudge Brownie 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0961-2013·2013-02-06

    Knott's Chicken Salad Recalled Due to Listeria Monocytogenes Contamination

    Knott's Wholesale Foods is recalling chicken salad sandwiches because a sample tested positive for Listeria Monocytogenes. The product was distributed in Tennessee and Kentucky.

    Product
    Knott's FINE FOODS, CHICKEN SALAD (sandwich), KNOTT's WHOLESALE FOODS, INC. 125 North Blakemore, Paris, TENNESSEE 38242, (731) 642-1961 www.knotsfoods.com, UPC 011984011326
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-138-2013·2013-02-06

    Qualitest Recalls Hydrocodone and Acetaminophen Tablets Due to Oversized Size

    Qualitest Pharmaceuticals is recalling 897,379 bottles of Hydrocodone bitartrate and acetaminophen tablets because a complaint reported the tablets were oversized.

    Product
    Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16; b) 60-count bottles, NDC 0603-3888-20; c) 90-count bottles, NDC 0603-3888-02; d) 100-count bottles, NDC 0603-3888-21; e) 120-count bottles, NDC 0603-3888-22…
    Category
    Drug
    Distribution
    Distributed nationwide