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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30851–30875 of 39756

  • SevereFDA (Drugs)·D-1524-2014·2014-08-13

    FDA Recalls Unapproved Vitamin B12 Injections Due to Unregistered Manufacturer

    Medical Supply Liquidators LLC is recalling Vitamin B12 Methylcobalamin 5000 Injection USP because the manufacturer is not registered with the FDA.

    Product
    Vitamin B12 Methylcobalamin 5000 Injection USP 5000 mcg/ml, 10 ml vial and 30 ml vial, Sterile, for IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1512-2014·2014-08-13

    Alexion Recalls Soliris Vials Due to Visible Particulate Matter

    Alexion Pharmaceuticals is recalling 96,506 vials of Soliris (eculizumab) because the product failed appearance tests for visible particles under labeled storage conditions.

    Product
    SOLIRIS — SOLIRIS (ECULIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1514-2014·2014-08-13

    Janssen Recalls Risperdal CONSTA Due to Sterility Failure

    Janssen Pharmaceuticals is recalling one lot of Risperdal CONSTA (risperidone) 25 mg dose packs due to a sterility failure detected in a stability sample.

    Product
    RISPERDAL CONSTA — RISPERDAL CONSTA (RISPERIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2296-2014·2014-08-13

    Hot Mama's Foods Recalls Hummus and Dip for Listeria Concerns

    Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes contamination.

    Product
    Roasted Garlic Hummus sold under the Archer Farms brand and packaged in a transparent plastic tub with a net weight of 17 oz (1 lb. 1 oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1523-2014·2014-08-13

    FDA Recalls Unapproved Vitamin B6 Injection Vials Nationwide

    Medical Supply Liquidators LLC is recalling Vitamin B6 Pyridoxine HCL for Injection because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.

    Product
    Vitamin B6 Pyridoxine HCL for Injection USP, 100 mg/ml, Sterile, for IM or Deep SQ Use, Multiple Dose 30 ml vial, manufactured by: CB Inc. for Sunshine Labs, www. sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V500000·2014-08-13

    GM Recalls 2011-2014 Chevrolet Express and GMC Savana CNG Vehicles

    General Motors is recalling 2011-2014 Chevrolet Express and GMC Savana CNG vehicles due to a potential natural gas leak that could cause a fire or explosion.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2290-2014·2014-08-13

    KIND Recalls Multiple Protein Bars Due to Potential Peanut Presence

    KIND, LLC is recalling several Strong & Kind and Kind protein bars nationwide and in Mexico due to the potential presence of peanut protein.

    Product
    STRONG & KIND Honey Smoked BBQ Almond Protein Bar, 45g, packaged in a red, black and transparent wrapper. Sold individually or packaged in a box of 4 or 12.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1531-2014·2014-08-13

    FDA Recalls G.A.C. 375 Injection Due to Unregistered Manufacturer

    The FDA is recalling G.A.C. 375 Injection USP because the manufacturing firm is not registered with the FDA as a drug manufacturer.

    Product
    G.A.C. 375 Injection USP, packaged in 30 ml vials, Sterile, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1529-2014·2014-08-13

    FDA Recalls Unapproved Vitamin B12 Injection Vials

    Medical Supply Liquidators LLC is recalling Vitamin B12 Hydroxocobalamin Injection vials because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.

    Product
    Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml, Sterile, 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2159-2014·2014-08-13

    ICU Medical Recalls Arterial Monitoring Kits Due to Fluid Leak Risk

    ICU Medical is recalling specific arterial monitoring kits because a component connection may crack, causing a fluid leak.

    Product
    Arterial Safeset Transpac IT w/3 ml Reservoir and Single CSP, With Velcro Arm Strap, Patient Mount, Item No. 011-46104-42 Transpac Trifurcated monitoring kit with Safeset Reservoir, squeeze flush and sampling ports. The monitoring kit is intended for measuring and montoring…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1532-2014·2014-08-13

    L-Carnitine Injection Recalled for Lack of FDA Approval and Registration

    Medical Supply Liquidators LLC is recalling L-Carnitine Injection USP 100 mg/ml because it was marketed without an approved NDA/ANDA and the manufacturer is not registered with the FDA.

    Product
    L-Carnitine Injection USP 100 mg/ml, packaged in 30 ml vials, Sterile, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1528-2014·2014-08-13

    B Complex Injection Recalled for Lack of FDA Approval

    Medical Supply Liquidators LLC is recalling B Complex for Injection USP with Methylcobalamin because it was marketed without an approved NDA/ANDA and the manufacturer is not FDA-registered.

    Product
    B Complex for Injection USP with Methylcobalamin 1000 mcg/ml, Sterile, for IM or Deep SQ use, multiple dose vial, packaged in 10 ml vials and 30 ml vials. Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2293-2014·2014-08-13

    KIND Recalls Multiple Protein Bars Due to Peanut Allergen

    KIND, LLC is recalling several KIND and Strong & KIND bar varieties due to the potential presence of peanut protein.

    Product
    STRONG & KIND Hickory Smoked Almond Protein Bar, 45g, packaged in a grey, black and transparent wrapper. Sold individually or packaged in a box of 4 or 12.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1521-2014·2014-08-13

    BCAA 4% Injection Recalled for Lack of FDA Approval

    Medical Supply Liquidators LLC is recalling BCAA 4% Branched Chain Amino Acid Injection USP because it was marketed without an approved NDA/ANDA and the manufacturer is not FDA-registered.

    Product
    BCAA 4% Branched Chain Amino Acid Injection USP, Sterile, 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2294-2014·2014-08-13

    KIND Recalls Multiple Protein Bars Due to Potential Peanut Presence

    KIND, LLC is recalling several protein bar varieties nationwide and in Mexico due to the potential presence of peanut protein.

    Product
    STRONG & KIND Thai Sweet Chili Almond Protein Bar, 45g, packaged in a purple, black and transparent wrapper. Sold individually or packaged in a box of 4 or 12.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2289-2014·2014-08-13

    KIND Bars Recalled Due to Potential Peanut Protein Presence

    KIND, LLC is recalling specific lots of KIND Healthy Grains Maple Pumpkin Seed Bars and other bars due to the potential presence of undeclared peanut protein.

    Product
    KIND HEALTHY GRAINS Maple Pumpkin Seed Bar, 35g, packaged in a purple, black and transparent wrapper. Sold individually or packaged in a box of 5.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1526-2014·2014-08-13

    Unapproved Injectable B Complex Recall Due to Unregistered Manufacturer

    Medical Supply Liquidators LLC is recalling Super MIC B Complex injections because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.

    Product
    Super MIC B Complex for L-Carnitine for Injection USP with Methylcobalamin 1000 mcg/ml, Sterile, for IM or Deep SQ Use, Multiple Dose Vial. Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1530-2014·2014-08-13

    FDA Recalls Unapproved Lipo 8 Injection Vials Due to Unregistered Manufacturer

    Medical Supply Liquidators LLC is recalling Lipo 8 Injection USP 200 mg/ml vials because the manufacturer is not registered with the FDA and the product lacks an approved NDA/ANDA.

    Product
    Lipo 8 Injection USP 200 mg/ml, packaged in 30 ml vials, Sterile, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V705000·2014-08-12

    Blue Bird Recalls 2015 School Buses Due to Fuel Filter Defect

    Blue Bird is recalling 2015 All American and Vision school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T010000·2014-08-12

    TBC Recalls Wild Country Radial Tires Due to Sidewall Cracking

    TBC Corporation is recalling specific Wild Country Radial XTX Sport tires due to sidewall cracking that could lead to sudden air loss and a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T009000·2014-08-11

    Continental Recalls Motorcycle Tires Due to Tread Separation Risk

    Continental is recalling specific motorcycle tires because the tread, belt, and carcass may separate, causing a loss of inflation pressure and increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V496000·2014-08-11

    Versalift Recalls Ford Super Duty Trucks with Fire Risk

    Versalift is recalling 2009-2013 Ford Super Duty trucks equipped with specific PTO assemblies due to a risk of fire from oil leaking onto the exhaust.

    Product
    FORD — FORD F-550 SUPER DUTY, F-350 SUPER DUTY, F-450 SUPER DUTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E052000·2014-08-08

    Lippert Recalls Recreational Vehicle Frames With Defective Spring Hangers

    Lippert is recalling certain recreational vehicle frames manufactured in February 2014 because the spring hangers may fracture, potentially causing loss of vehicle control.

    Product
    STRUCTURE:FRAME AND MEMBERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V490000·2014-08-08

    General Motors Recalls 2002-2004 Saturn Vues for Ignition Key Defect

    General Motors is recalling 2002-2004 Saturn Vues because the key may be removed from the ignition while the vehicle is not in the Off position, creating a risk of the vehicle rolling away.

    Product
    SATURN — SATURN VUE
    Category
    Vehicle
    Distribution
    Distributed nationwide