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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31701–31725 of 39756

  • SevereFDA (Devices)·Z-1060-2014·2014-03-12

    McKesson Anesthesia Care System Recalled for Data Mismatch

    McKesson Technologies is recalling 10 units of the Anesthesia Care system because patient case data did not match the patient data, including data from another case.

    Product
    McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1610-2014·2014-03-12

    Dairy Rich Chocolate Ice Cream Recalled for Potential Peanut Allergen

    Ice Cream Specialities is voluntarily recalling Dairy Rich Chocolate Ice Cream because it may contain peanut butter, a peanut allergen.

    Product
    Chocolate Ice Cream manufactured under the Dairy Rich brand and packaged in a 1.75 quart (1.66 L) (56 oz.) carton.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1148-2014·2014-03-12

    Fresenius Kabi Recalls Heparin Sodium Injection Due to Subpotency

    Fresenius Kabi is recalling Heparin Sodium Injection vials because they may contain less active ingredient than labeled.

    Product
    HEPARIN SODIUM — HEPARIN SODIUM (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1101-2014·2014-03-12

    Bladder Instillation Recalled for Lack of Sterility Assurance

    Natures Pharmacy & Compounding Center is recalling all lots of Bladder Instillation due to quality control concerns affecting sterility assurance.

    Product
    Bladder Instillation
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1102-2014·2014-03-12

    Bleomycin Sulfate Recalled Due to Sterility Assurance Concerns

    Natures Pharmacy & Compounding Center is recalling all non-expired lots of Bleomycin Sulfate 1unit/ml due to quality control issues affecting sterility assurance.

    Product
    Bleomycin Sulfate 1unit/ml
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1150-2014·2014-03-12

    Shimadzu Recalls Mobile X-ray Systems Due to Metal Plate Cracking Risk

    Shimadzu Medical Systems is recalling 56 mobile X-ray systems because a connecting metal plate may crack, posing a structural safety risk.

    Product
    Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1621-2014·2014-03-12

    Mandarin Orange Tozzetti Biscotti Recalled for Undeclared Allergens

    Yukon Concessions Alaska LLC is recalling Mandarin Orange Tozzetti Biscotti due to undeclared wheat, soy, and milk.

    Product
    Mandarin Orange Tozzetti Biscotti - individually wrapped in cellophane. Product is sold under Tonia's Biscotti brand, net wt. 2 oz.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1598-2014·2014-03-12

    Rise n Roll Bakery Recalls Cinnamon Caramel Donuts for Undeclared Egg

    Rise'n Roll Bakery is recalling Cinnamon Caramel Donuts and Donut Holes because they contain an undeclared egg ingredient. The products were sold in multiple states and online.

    Product
    Rise n Roll Bakery & Deli, Cinnamon Caramel Donuts, sold individually and found in 6 count (436 g) UPC Code 6 26570 61744 0 or 12 count (861.83 g) UPC Code 6 26570 617457, variety donut box identifying all donut varieties and in Cinnamon Caramel Donut Holes, 1.05 lb, UPC Code…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-1105-2014·2014-03-12

    Natures Pharmacy Recalls Cyano B-12 Due to Sterility Concerns

    Natures Pharmacy & Compounding Center is recalling Cyano B-12 (Cmpd) 1000mcg/ml due to quality control issues affecting sterility assurance.

    Product
    Cyano B-12 (Cmpd) 1000mcg/ml
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1599-2014·2014-03-12

    Rise n Roll Bakery Recalls Glazed Donuts for Undeclared Egg

    Rise'n Roll Bakery is recalling glazed donuts because they contain egg, which is not listed on the label.

    Product
    Rise n Roll Bakery & Deli, Glazed Donuts, sold individually and found in 6 count (436 g) UPC Code 6 26570 61744 0 or 12 count (861.83 g) UPC Code 6 26570 617457, variety donut box identifying all donut varieties Glazed Donuts Enriched wheat flour, soybean oil, dextrose…
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·14V120000·2014-03-12

    Keystone Recalls 2014 Fifth Wheels and Travel Trailers for Axle Bearing Defect

    Keystone is recalling specific 2014 fifth wheels and travel trailers because insufficient lubrication in the inner wheel bearings may cause the wheel to seize or separate, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE BULLET, SPRINGDALE, PASSPORT, HIDEOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1612-2014·2014-03-12

    Yukon Concessions Recalls Lemon Biscotti for Undeclared Allergens

    Yukon Concessions Alaska LLC is recalling Lemon Biscotti dipped in White Chocolate due to undeclared wheat, soy, and milk.

    Product
    Lemon Biscotti dipped in White Chocolate Bag, 13 oz., sold in white windowed paper coated bakery bags, And individually wrapped in cellophane - net wt. 2 oz.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1616-2014·2014-03-12

    Tonia's Biscotti Recalled for Undeclared Wheat, Soy, and Milk Allergens

    Yukon Concessions Alaska LLC is recalling Tonia's Biscotti Traditional Toasted Almond Biscotti due to undeclared wheat, soy, and milk.

    Product
    Traditional Toasted Almond Biscotti-individually wrapped in cellophane. Product is sold under Tonia's Biscotti brand, net wt. 2 oz.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1136-2014·2014-03-12

    Terbutaline/Ipratropium Recall Due to Sterility Assurance Concerns

    Natures Pharmacy & Compounding Center is recalling all lots of Terbutaline/Ipratropium 0.5mg/2.5ml due to quality control issues affecting sterility assurance.

    Product
    Terbutaline/Ipratropium 0.5mg/2.5ml
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1109-2014·2014-03-12

    FDA Recalls Estradiol and Testosterone Compounds for Sterility Concerns

    Natures Pharmacy & Compounding Center is recalling all lots of Estradiol Cypionate and Testosterone Cypionate due to sterility assurance concerns identified during an FDA inspection.

    Product
    Estradiol Cypionate 2mg/cc testosterone cypionoate 50mg
    Category
    Drug
    Distribution
    1 state