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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31751–31775 of 39756

  • SevereNHTSA·14V102000·2014-03-10

    Starcraft Prodigy and Quest School Buses Recalled for Door Actuator Fire Risk

    Starcraft Bus is recalling 281 model year 2009 and 2010 Prodigy and Quest school buses because voltage spikes may damage door actuator circuit boards, increasing the risk of a fire.

    Product
    STARCRAFT — STARCRAFT PRODIGY, QUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V108000·2014-03-07

    Eldorado Transit Bus Recall for Exhaust Fire Risk

    Eldorado is recalling certain transit buses because condensation in the engine intake may freeze, causing exhaust flames that risk fire or burn injuries.

    Product
    ENC — ENC XHF, EZ-RIDER II, AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V111000·2014-03-07

    CM Trailers Recalls 2012 Cargo Van and Revolution Trailers for Brake Defect

    CM Trailers is recalling 2012 Cargo Van and Revolution trailers because a manufacturing defect in the hydraulic brake pump could cause a loss of braking ability.

    Product
    CM TRAILERS — CM TRAILERS CARGO VAN, REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·018-2014·2014-03-07

    George's Recalls Chicken Breast Strips Due to Undeclared Soy Allergen

    George's Inc. is recalling 29,200 pounds of seasoned raw chicken breast strips because the labels failed to declare soy protein and MSG.

    Product
    George's Further Processing — Arkansas Firm Recalls Chicken Products Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·14E007000·2014-03-07

    Gates Recalls Tru-Flow Water Pumps for Timing Belt Failure Risk

    Gates is recalling specific aftermarket Tru-Flow water pumps for Audi and Volkswagen vehicles because the pulley may develop microfractures, causing the timing belt to fail and the engine to shut down.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI BEETLE, A4, TT, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14125·2014-03-06

    Packaging Tape Recalls Air Movers Due to Fire Hazard

    Packaging Tape is recalling about 2,800 air movers sold from 2008 to 2010 because a thermal switch failure can cause the motor to overheat and start a fire.

    Product
    Air movers/blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0957-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port and Preloaded Stylet, 6.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1548-2014·2014-03-05

    UNFI Recalls Kinnikinnick Waffles Due to Undeclared Milk Allergen

    UNFI is recalling Kinnikinnick Original Homestyle Waffles nationwide because the product contains undeclared milk. Consumers should stop eating the product and return it to the store.

    Product
    Kinnikinnick Original Homestyle Waffles-Weight: 210 g/7.4oz Qty/Pkg: 6 Cardboard Box-UPC: 62013300198 1
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0950-2014·2014-03-05

    Teleflex Recalls ISIS HVT Tracheal Tubes Due to Kinking Risk

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 6.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0951-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Hazard

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during use, potentially compromising the patient's airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 6.5, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0956-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 9.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1543-2014·2014-03-05

    The Cultured Kitchen Recalls Smoked Cheddar Cashew Cheese for Salmonella Risk

    The Cultured Kitchen is recalling Smoked Cheddar Cashew Cheese due to potential Salmonella contamination. Affected products have expiry dates up to and including April 19, 2014.

    Product
    The Cultured Kitchen Smoked Cheddar Cashew Cheese; Processed raw at low temperatures to preserve minerals, enzymes and nutrients. Wheat, dairy, soy and gluten free. This product contains live active cultures Keep Refrigerated 8 oz., (226.8 grams) Plastic container UPC…
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1544-2014·2014-03-05

    The Cultured Kitchen Recalls Pepper Jack Cashew Cheese Due to Salmonella Risk

    The Cultured Kitchen is recalling Pepper Jack Cashew Cheese due to potential Salmonella contamination. Affected products have expiry dates up to and including April 19, 2014.

    Product
    The Cultured Kitchen Pepper Jack Cashew Cheese; Processed raw at low temperatures to preserve minerals, enzymes and nutrients. Wheat, dairy, soy and gluten free. This product contains live active cultures Keep Refrigerated 8 oz., (226.8 grams) Plastic container UPC…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0952-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 7.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0954-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Hazard

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 8.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1549-2014·2014-03-05

    UNFI Recalls Kinnikinnick Waffles for Undeclared Milk Allergen

    UNFI is recalling Kinnikinnick Cinnamon & Brown Sugar Homestyle Waffles nationwide due to undeclared milk. The recall is voluntary and classified as Class I.

    Product
    Kinnikinnick Cinnamon & Brown Sugar Homestyle Waffles-Weight: 210 g/7.4oz Qty/Pkg: 6 Cardboard Box-UPC: 62013300199 8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1071-2014·2014-03-05

    GE Healthcare Recalls Infant Resuscitation Systems Due to Reversed Fittings

    GE Healthcare is recalling Giraffe and Panda infant resuscitation systems because oxygen and air inlet fittings were reversed during assembly.

    Product
    GE Healthcare - Giraffe and Panda Bag and Mask Resuscitation System;Giraffe Stand-alone Infant Resuscitation System. Product Usage: The Bag and Mask Resuscitation System provides the basic equipment required for pulmonary resuscitation of infants. Pulmonary resuscitation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1090-2014·2014-03-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for ESD Component Damage

    Philips is recalling HeartStart MRx Monitor/Defibrillators because a processor board component may be damaged by electrostatic discharge, disrupting ECG and SpO2 functionality.

    Product
    HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0963-2014·2014-03-05

    Teleflex ISIS HVT Tracheal Tubes Recalled for Kinking Risk

    Teleflex Medical is recalling ISIS HVT Tracheal Tubes because they can kink during patient use, potentially compromising the airway.

    Product
    ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port and Preloaded Stylet, 9.0, Rx only, Product Usage: A tracheal tube is a device inserted into a patients trachea via the nose or mouth and used to maintain an open airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1050-2014·2014-03-05

    Medline Recalls Surgical Kits With Flaking Guidewire Coating

    Medline Industries is recalling 304 surgical kits containing guidewires with a potential for coating to flake off.

    Product
    CATH TRAY; REF: DYNJ41101; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1046-2014·2014-03-05

    Medline Recalls Angiography Packs Due to Guidewire Coating Flaking Risk

    Medline Industries is recalling 1,194 angiography packs because a guidewire component may have flaking coating. The recall covers distribution in seven US states.

    Product
    ANGIOGRAPHY PACK; REF: DYNJ26855D; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1554-2014·2014-03-05

    Kinnikinnick Pancake and Waffle Mix Recalled for Undeclared Milk

    Bozzutos Inc. is recalling Kinnikinnick Pancake & Waffle Mix due to undeclared milk, a major food allergen.

    Product
    Kinnikinnick Pancake & Waffle Mix -Weight: 454g/16 oz Cardboard Box UPC 62013310512 2
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1069-2014·2014-03-05

    Terumo Recalls VirtuoSaph Plus Endoscopic Vessel Harvesting System

    Terumo is recalling 26 units of the VirtuoSaph Plus Endoscopic Vessel Harvesting System due to potential sterility compromise.

    Product
    VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only*** Product Usage: The VirtuoSaph  Plus Endoscopic Vessel Harvesting System is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1089-2014·2014-03-05

    Caraco Recalls Metformin HCl ER Tablets Due to Foreign Tablet Presence

    Caraco Pharmaceutical is recalling 2,528 bottles of Metformin HCl ER 500 mg tablets because a customer reported finding Gabapentin tablets in the bottle.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide