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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Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

31926–31950 of 39756

  • SevereFDA (Devices)·Z-0860-2014·2014-02-05

    Codman Certas Programmable Valves Recalled for Potential Malfunction

    Codman & Shurtleff, Inc. is recalling 431 Codman Certas Programmable Valves because they may not operate properly. These implantable devices are used to manage hydrocephalus.

    Product
    Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal Catheter and Accessories Product Code: 82-8803 Product Usage: The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1461-2014·2014-02-05

    YOR Digest Ultra Recalled Due to Chloramphenicol Contamination

    Health Wright Products Inc. is recalling YOR Digest Ultra dietary supplements because they were made with ingredients contaminated with Chloramphenicol.

    Product
    Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1458-2014·2014-02-05

    Digestaze dietary supplement recalled due to Chloramphenicol contamination

    Health Wright Products Inc is recalling Digestaze dietary supplements because they were made from an ingredient contaminated with Chloramphenicol.

    Product
    Digestaze, dietary supplement, 90 vegetable capsules per bottle. They are sold under brand DESBIO
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1035-2014·2014-02-05

    Hospira Recalls Aminosyn 3.5% Bags Due to Sterility Concerns

    Hospira Inc. is recalling 15,258 bags of Aminosyn 3.5% M Sulfite-Free due to a lack of assurance of sterility and potential leakage from the administrative port.

    Product
    Aminosyn 3.5% M Sulfite-Free, A Crystalline Amino Acid Solution* with Maintenance Electrolytes with Phosphorus, 1000 mL bag, Rx only. Hospira Inc, Lake Forest, IL, 60045. NDC: 0409-4196-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1036-2014·2014-02-05

    Hospira Recalls Heparin Sodium Bags Due to Sterility Concerns

    Hospira is recalling 27,780 bags of Heparin Sodium 2000 USP Units per 1000 mL due to a lack of assurance of sterility and potential leakage from the administrative port.

    Product
    HEPARIN SODIUM — HEPARIN SODIUM (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1460-2014·2014-02-05

    Health Wright Recalls XymoZyme Dietary Supplements Due to Chloramphenicol Contamination

    Health Wright Products Inc is recalling XymoZyme dietary supplements because the ingredients were contaminated with Chloramphenicol. The affected products were distributed to California, Florida, Oregon, Utah, and Mexico.

    Product
    XymoZyme, dietary supplement, packaged 60 capsules per bottte, 120 capsules per bottle, sold under brand ZYMOGEN.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0835-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 121 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Knee/Shoulder Blanket NS, REF T652NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2014·2014-02-04

    ConAgra Recalls Chicken Noodle Soup for Undeclared Wheat and Egg Allergens

    ConAgra Foods is recalling 54,673 pounds of chicken noodle soup mislabeled as chicken with rice, failing to declare wheat and egg allergens.

    Product
    Pennsylvania Firm Recalls Chicken Noodle Soup Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·14V031000·2014-02-04

    Mitsubishi Recalls 2013 Outlander Sport for Air Bag Wiring Defect

    Mitsubishi is recalling 2013 Outlander Sport vehicles with leather seats because improperly routed air bag wiring may prevent the driver's air bag from deploying in a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V035000·2014-02-04

    Schwing Recalls 2012-2013 Concrete Pump Trucks Due to Fire Risk

    Schwing America is recalling 2012-2013 concrete pump trucks because a specific potting compound in DC-DC converters can conduct electricity and cause fires.

    Product
    SCHWING — SCHWING S39SX, S58SX, S61SX, S43SX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V034000·2014-02-04

    Chrysler Recalls 2014 Ram ProMaster Vehicles for Brake Hose Defect

    Chrysler is recalling 2014 Ram ProMaster vehicles because a manufacturing tool may have damaged a brake hose, potentially causing fluid leakage and reduced braking performance.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·010-2014·2014-02-04

    Texas Firm Recalls Beef Products Due To Possible E. Coli Contamination

    PFP Enterprises is recalling approximately 15,865 pounds of beef products distributed in four states and Puerto Rico due to possible contamination with multiple non-O157 E. coli strains.

    Product
    Texas Firm Recalls Beef Products Due To Possible E. Coli Contamination
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·14V037000·2014-02-04

    Kaffenbarger Recalls International Trucks with Fire-Prone DC-DC Converters

    Kaffenbarger is recalling certain 2006-2013 International trucks because a specific DC-DC converter potting compound can conduct electricity and cause a fire.

    Product
    INTERNATIONAL — INTERNATIONAL 9900I SFA 6X4, 7600 SFA 6X4, 4300 SBA 4X2, 4300M7 SBA 4X2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·008-2014·2014-01-30

    Walker's Recalls Chicken Salad Products Due to Undeclared Soy Allergen

    Walker's Food Products is recalling chicken salad products because they contain soy protein concentrate, a known allergen, that was not declared on the labels.

    Product
    Walker's Food Products Co. — Missouri Firm Recalls Chicken Salad Products Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·14V026000·2014-01-30

    Kenworth T370 Recall for Transmission Software Defect

    PACCAR is recalling 2014 Kenworth T370 chassis with Eaton hybrid transmissions because software may cause unintended acceleration.

    Product
    KENWORTH — KENWORTH T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14098·2014-01-30

    Britax Recalls Strollers Due to Fingertip Amputation Hazard

    Britax is recalling B-Agile and BOB Motion strollers because the folding mechanism can amputate fingertips or break fingers.

    Product
    B-Agile, B-Agile Double and BOB Motion strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14095·2014-01-30

    Gree Recalls GE Brand Dehumidifiers Due to Fire and Burn Hazards

    Gree is expanding its recall to include GE-brand dehumidifiers that can overheat, smoke, and catch fire. Consumers should unplug the units and contact Gree for a refund.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1437-2014·2014-01-29

    Flat Creek Farm Recalls Raw Milk Blue Cheese Due to Salmonella

    Flat Creek Farm & Dairy is recalling Heavenly Blue raw milk cheese contaminated with Salmonella. The product was distributed in Alabama, Florida, Georgia, and Tennessee.

    Product
    Heavenly Blue, (Raw milk, salt, culture, coagulant ), Flat Creek Lodge, 367 Bishop Chapel Church Rd, Swainsboro, GA 30401. The raw milk blue cheese is packaged in clear plastic, with sizes ranging from 1/2 lb to whole wheels.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-893-2014·2014-01-29

    FDA Recalls Tizanidine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Tizanidine HCl 2 mg tablets that may have been mislabeled as Niacin TR 500 mg.

    Product
    tiZANidine HCl, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378072219.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-940-2014·2014-01-29

    Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Pyridoxine HCL 25 mg tablets because they may have been mislabeled as Torsemide 10 mg.

    Product
    PYRIDOXINE HCL, Tablet, 25 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536440601.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0788-2014·2014-01-29

    Codman TRUFILL n-BCA Liquid Embolic System Recalled for Incorrect Instructions

    Codman & Shurtleff, Inc. is recalling 3,860 units of the TRUFILL n-BCA Liquid Embolic System due to incorrect instructions for use.

    Product
    TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-400; The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-847-2014·2014-01-29

    Venlafaxine HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Venlafaxine HCL 100 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    VENLAFAXINE HCL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093738301.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-959-2014·2014-01-29

    FDA Recalls Hyoscyamine Sulfate Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling 909 tablets of Hyoscyamine Sulfate SL 0.125 mg because they may have been mislabeled as other prescription drugs.

    Product
    HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574025001.
    Category
    Drug
    Distribution
    4 states