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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Minimum severity

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

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34926–34950 of 39756

  • SevereFDA (Devices)·Z-1190-2013·2013-05-08

    Medtronic Recalls Deep Brain Stimulation Lead Kits Due to Damage Risk

    Medtronic is recalling 30,000 Deep Brain Stimulation lead kits worldwide because the provided lead cap may damage the lead connector during use.

    Product
    Medtronic DBS Lead Kit for Deep Brain Stimulation, models 3387, 3387S, 3389, 3389S, 3391, 3391S. Sterile and Non-Pyrogenic. Product Usage: The deep brain stimulation system delivers electrical stimulation to selected targets in the brain. DBS Leads are indicated for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1367-2013·2013-05-08

    Rich Products Recalls Mozzarella Bites for E. coli O121 Contamination

    Rich Products Corp is recalling Mozzarella Bites potentially contaminated with E. coli O121. The recall covers 820,577 cases distributed nationwide.

    Product
    Mozzarella Bites distributed under the following labels: Farm Rich Cheese In a Pizzeria Style Crust, Product Code 36450 Net Wt. 22-oz bag-UPC Code 0 41322 37443 1; Product Code 37443 Net Wt. 22-oz bag-UPC Code 0 41322 37443 1; Product Code 37433 Net Wt. 22-oz bag-UPC Code 0…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1376-2013·2013-05-08

    Buffalo Trace Hot Barbeque Sauce Recalled for Missing Allergen Labels

    Buffalo Trace Distillery is recalling 16 fl. oz. jars of Hot Barbeque Sauce because the labels failed to list soy and anchovy allergens.

    Product
    BUFFALO TRACE HOT BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: [email protected] website…
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-1374-2013·2013-05-08

    Buffalo Trace Meat Marinade Recalled for Missing Wheat and Anchovy Allergens

    Buffalo Trace Distillery is recalling 12 fl. oz. meat marinade bottles because the label failed to list wheat and anchovy allergens.

    Product
    BUFFALO TRACE MARINADE FOR MEAT Net Wt. 12 fl. oz. PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: [email protected] website…
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-1370-2013·2013-05-08

    Farm Rich Pizza Dippers Recalled for Potential E. coli O121 Contamination

    Rich Products Corp is recalling Farm Rich Better For You Pizza Dippers nationwide due to potential E. coli O121 contamination.

    Product
    Farm Rich Better For You Pizza Dippers-Pizza Dough Stuffed with Reduced Fat Mozzarella Cheese, Net Wt 25-LBS (5 X 5-LB), UPC Code 10041322652338, Product Code 65233.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1185-2013·2013-05-08

    Medi-Trace Pediatric Defibrillation Electrodes Recalled for Arcing Risk

    FDA is recalling Medi-Trace Cadence Pediatric Defibrillation Electrodes because arcing or sparking may damage the leadwire, preventing the device from delivering appropriate energy to patients.

    Product
    Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1160-2013·2013-05-08

    Hospira Recalls GemStar Infusion Pumps Due to Battery Data Loss

    Hospira is recalling GemStar infusion pumps because low battery levels can corrupt data and cause an error that prevents the device from being used.

    Product
    GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1372-2013·2013-05-08

    Buffalo Trace Bourbon Flavored Caramel Sauce Recalled for Missing Milk Allergen Label

    Buffalo Trace Distillery is recalling 1,504 jars of Bourbon Flavored Caramel Sauce because the label failed to list milk as an allergen.

    Product
    BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail…
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-309-2013·2013-05-08

    Hospira Recalls Diazepam Injection Vials Due to Sterility Concerns

    Hospira Inc. is recalling 172,350 vials of Diazepam Injection due to a loose crimp on the fliptop vial that compromises sterility assurance.

    Product
    DIAZEPAM — DIAZEPAM (DIAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1366-2013·2013-05-08

    Wegmans Recalls Roasted Red Pepper Dip Due to Missing Allergen Labeling

    Wegmans is recalling Roasted Red Pepper Dip because some containers have incorrect labels that fail to list milk and eggs.

    Product
    Wegmans Food You Feel Good About Roasted Red Pepper Dip, Net Wt 8 oz. (227g) Product is packaged in plastic containers, 12 containers per case. UPC: 77890 23286 with a best-by date of 5/17/2013. Commodity Code: 23286, Item #: DIPWG23286
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-311-2013·2013-05-08

    Axara Recalls Well at Walgreens Antacid Liquid Due to E. Coli Contamination

    Tarmac Products, Inc. is recalling specific lots of Well at Walgreens Regular Strength Antacid Liquid due to elevated microbial counts and E. Coli contamination.

    Product
    "Well at Wallgreens" Regular Strength Antacid Liquid (Alumina/Magnesia/Simethicone/Antacid & Anti Gas); Mint, a)12 oz bottle (NDC 0363-0073-02), b) 26 oz. bottle (NDC 0363-0073-26), Distributed by Walgreens CO., 200 Wilmot Rd, Deerfield, IL 60015.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1171-2013·2013-05-08

    Newport Medical Instruments Recalls HT70 Ventilator Power Pac Batteries

    Newport Medical Instruments is voluntarily recalling HT70 and HT70 Plus ventilator Power Pac batteries because they may cause the ventilator to alarm and switch to backup power sooner than expected.

    Product
    Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries Model number: HT70 and HT70 Plus. The HT70 and HT70 Plus ventilator systems are intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of…
    Category
    Medical Device
    Distribution
    39 states
  • SevereNHTSA·13V184000·2013-05-08

    Autocar Recalls 2005-2013 Trucks Due to Missing Air Brake Drain Valves

    Autocar is recalling 82 model year 2005-2013 ACX, WX, and WXLL trucks because their air brake systems lack required drain valves, potentially reducing brake performance.

    Product
    AUTOCAR — AUTOCAR WXLL, WX, ACX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V179000·2013-05-07

    Lion Bus Recalls One 2014 Model 360 Bus for Brake Line Chafing

    Lion Bus is recalling one 2014 model year 360 bus because the air compressor and hydraulic brake lines may chafe, causing a hole in the brake line and increasing crash risk.

    Product
    LION — LION 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V175000·2013-05-07

    Chrysler Recalls Jeep Grand Cherokee and Commander for Electrical Defect

    Chrysler is recalling 2005-2010 Jeep Grand Cherokee and 2006-2010 Jeep Commander vehicles because an electrical failure may cause the transfer case to shift into neutral, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V174000·2013-05-06

    Dutchmen Recalls 2013 Breckenridge RVs Due to Awning Motor Defect

    Dutchmen is recalling 2013 Breckenridge recreational vehicles because an awning motor defect may cause the awning to unfurl unexpectedly, increasing the risk of injury or a crash.

    Product
    BRECKENRIDGE — BRECKENRIDGE BRECKENRIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13182·2013-05-02

    LEM 5-Tray Food Dehydrators Recalled Due to Fire Hazard

    LEM Products Distribution is recalling 5-Tray Food Dehydrators because a fan failure can cause the unit to overheat and start a fire. Consumers should stop using the product and contact the company for repair.

    Product
    5-Tray Dehydrator with Digital Timer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V172000·2013-05-02

    BMW Recalls 2002-2003 Models Due to Passenger Air Bag Defect

    BMW is recalling 2002-2003 models because the passenger air bag inflator may rupture, sending metal fragments into the cabin during a crash.

    Product
    BMW — BMW 325XI, 325IT, M3, 325XIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-267-2013·2013-05-01

    Dietary Supplement Recalled for Undeclared Drug Ingredients

    Brower Enterprises Inc. is recalling WOW Health Enterprises Dietary Supplement because it contains undeclared drug ingredients, making it an unapproved drug.

    Product
    WOW, Health Enterprises, Dietary Supplement, 30 Caplets, Distributed by: Health Enterprises, 1002 E 5th St., Canton, SD 57013. Manufactured by Riger Natural, S. A. Mexico.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-283-2013·2013-05-01

    BiMix Standard Injectable Recalled for Lack of Sterility Assurance

    Axium Healthcare Pharmacy is recalling BiMix Standard Injectable due to lack of sterility assurance and quality control concerns.

    Product
    BiMix Standard Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-285-2013·2013-05-01

    FDA Recalls Quadmix Custom Injectable Due to Sterility Assurance Concerns

    Axium Healthcare Pharmacy is recalling Quadmix Custom Injectable vials due to lack of sterility assurance and quality control concerns.

    Product
    Quadmix Custom Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1347-2013·2013-05-01

    Wild Blue Yonder Recalls Gluten-Free Granola for Undeclared Almonds

    Wild Blue Yonder Foods is recalling Chappaqua Crunch GF Simply Granola with Flax & Fruit due to undeclared almonds. The product was distributed in nine states.

    Product
    Chappaqua Crunch GF(Gluten Free) Simply Granola with Flax & Fruit , 12 ounce pouch UPC: 786516-76002 6
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-281-2013·2013-05-01

    Axium Healthcare Recalls Mono-mix Injectable Due to Sterility Concerns

    Axium Healthcare Pharmacy is recalling Mono-mix (Prostaglandin) Injectable due to lack of assurance of sterility and quality control concerns.

    Product
    Mono-mix (Prostaglandin) Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states