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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29526–29550 of 39756

  • SevereUSDA FSIS·015-2015·2015-01-17

    Kalle USA Recalls Pork Products Produced Without Inspection

    Kalle USA is recalling approximately 168,473 pounds of dehydrated pork products that were not presented for U.S. inspection. No adverse reactions have been reported.

    Product
    Illinois Firm Recalls Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·014-2015(Original)·2015-01-17

    La Guadalupana Recalls Chicken Tamales Lacking Required Safety Plans

    La Guadalupana Wholesale is recalling 8,856 pounds of chicken tamales because they were produced without a required HACCP plan or Listeria program.

    Product
    La Guadalupana — Illinois Firm Recalls Chicken Products Produced Without Adequate Ready-To-Eat HACCP Plan and a Listeria Monocytogenes Program
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·011-2015·2015-01-16

    Buffalo Provisions Recalls Chorizo Products Due to Undeclared Peanut Allergen

    Buffalo Provisions is recalling approximately 48,210 pounds of chorizo products because they may contain undeclared peanuts. The products were distributed in Connecticut, New Jersey, and New York.

    Product
    New York Firm Recalls Chorizo Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • CriticalUSDA FSIS·012-2015·2015-01-16

    Kabobs Recalls Beef and Chicken Products Due to Undeclared Peanuts

    Kabobs Acquisition Inc. is recalling approximately 869 pounds of beef and chicken products because they may contain undeclared peanuts.

    Product
    Kabobs Aquisition, LLC — Georgia Firm Recalls Beef and Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    6 states
  • SevereUSDA FSIS·010-2015·2015-01-16

    Heywoods Tasso Pork Shoulder Recalled for Undeclared Peanuts

    Heywoods Meat Haus & Provision Co. is recalling 931 pounds of Tasso pork shoulder products due to misbranding and undeclared peanut allergens.

    Product
    The Heywoods Group Corp — Georgia Firm Recalls Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0768-2015·2015-01-14

    Gold Star Recalls Cold Smoked Steelhead Due to Listeria Contamination

    Gold Star Smoked Fish Corp. is recalling cold smoked steelhead due to Listeria monocytogenes contamination. The product was distributed in New York, New Jersey, and Florida.

    Product
    GOLD STAR'S FINEST COLD SMOKED STEELHEAD, Net Wt. (To Be Weighed At Time of Sale). UPC 021 143140026. Product is sold in a Vacuum Pack with blue and gold label. PERISHABLE. KEEP REFRIGERATED. Distributed by: Gold Star 570 Smith Street Brooklyn, NY 11231, 718-522-1545.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0905-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled Due to Fracture Risk

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.

    Product
    Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0767-2015·2015-01-14

    Azure Farm Organic Cilantro Flakes Recalled for Salmonella Risk

    K F K Seasonings LLC is recalling Azure Farm Organic Cilantro Flakes due to potential Salmonella contamination. The product was distributed in Oregon.

    Product
    Cilantro Flakes Organic, sold under private label Azure Farm, Net wt. 4 oz. or 1 lb. Product is packed in the heat seal poly bag. The 4 oz. bag has UPC 8 70722 00256 5. The 1 lb. bag has UPC 8 70722 00255 8. The 4 oz bag is labeled in parts: "***Cilantro Flakes…
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·009-2015·2015-01-14

    Agri Star Recalls Beef Franks for Undeclared Peanuts and Misbranding

    Agri Star Meat & Poultry is recalling 1,690 pounds of beef franks that may contain undeclared peanuts and are misbranded as gluten-free.

    Product
    Agri Star Meat and Poultry, LLC — Iowa Firm Recalls Beef Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0880-2015·2015-01-14

    Alere INRatio PT/INR Test Strips Recalled for Inaccurate Results

    Alere San Diego, Inc. is recalling INRatio PT/INR Test Strips because the system may provide INR results significantly lower than reference laboratory methods.

    Product
    Alere INRatio PT/INR Test Strips, Alere INRatio PT/INR System Professional - 0100071 Alere INRatio PT/INR Test Strips, Box of 12 - 0100139 Alere INRatio PT/INR Test Strips, Box of 48 The test strips are packaged in individually pouched test strips in a labeled box with 12…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0903-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled for Fracture Risk During Surgery

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.

    Product
    Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0904-2015·2015-01-14

    DePuy ATTUNE INTUITION Impactors Recalled Due to Fracture Risk

    DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they may break during knee surgery, potentially leaving small fragments in the patient.

    Product
    Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0921-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER U Remote Controls for Unintended Movement

    Trumpf Medical Systems is recalling JUPITER U remote controls because damaged units may cause unintended movement of operating tables during surgery.

    Product
    IR remote control JUPITER U, Material no. 4500120, Serial number: to (incl.) 102306940. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer…
    Category
    Medical Device
    Distribution
    25 states
  • SevereFDA (Devices)·Z-0881-2015·2015-01-14

    Alere INRatio Monitors Recalled for Potential Inaccurate INR Results

    Alere San Diego, Inc. is recalling INRatio PT/INR Monitor systems because they may provide INR results significantly lower than reference laboratory methods.

    Product
    INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional - 0100007 INRatio Prothrombin Time (PT) Monitoring System - 0100137 Alere INRatio Replacement Monitor The test systems contain individually packaged components needed to use the product, such as a monitor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0334-2015·2015-01-14

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira Inc. is recalling 30,840 bags of 0.9% Sodium Chloride Injection, USP, 100mL, due to a potential leak at the administrative port that compromises sterility.

    Product
    0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0882-2015·2015-01-14

    Alere INRatio 2 Monitors Recalled for Potential Inaccurate INR Results

    Alere San Diego, Inc. is recalling INRatio 2 PT/INR monitors because they may provide results significantly lower than reference laboratory methods.

    Product
    INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Testing System - 0200432 Alere INRatio 2 PT/INR Home Monitoring System - 0200433 Alere INRatio 2 PT/INR Home Monitoring System - 0200457 Alere INRatio 2 Replacement Monitor - 55112 Alere INRatio 2 Replacement…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V010000·2015-01-14

    Winnebago Recalls 2013-2015 Travel Trailers Due to Propane Leak Risk

    Winnebago is recalling specific 2013-2015 Minnie and Sunnybrook Remington travel trailers because the axle may crack the propane pipe fitting, creating a fire hazard.

    Product
    WINNEBAGO — WINNEBAGO, SUNNYBROOK MINNIE, REMINGTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2015·2015-01-14

    DePuy I.M. Hole Locator Instrument Recalled for Fracture Risk

    DePuy Orthopaedics is recalling 1,130 I.M. Hole Locator Instruments because excessive force during use may lead to intra-operative femoral fracture.

    Product
    I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. The IM Hole locator guides the IM drill during IM Hole preparation. The instrument is positioned between the condyles and aligned with the anatomical axis. Pins can be placed in the IM hole locator to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0931-2015·2015-01-14

    Synthes Small Electric Drive Recalled for Unintended Start and Malfunction

    Synthes (USA) Products LLC is recalling 12 Small Electric Drive units due to potential unintended starts or reverse mode failures that could cause tissue damage.

    Product
    Synthes Small Electric Drive (SED), part number: 05.001.175: The Small Electric Drive is designed for use in general traumatology, especially hand and food applications involving surgical procedures such as drilling, burring, reaming, pin and wire placement, cutting of bone and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2015·2015-01-14

    Trumpf Medical Systems Recalls IIR Remote Controls for Operating Tables

    Trumpf Medical Systems is recalling IIR remote controls for JUPITER operating tables due to reports of unintended movement during surgery.

    Product
    IIR remote control JUPITER, Material no.4544120, Serial number: to (incl.) 102006720. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer…
    Category
    Medical Device
    Distribution
    25 states
  • SevereFDA (Food)·F-0764-2015·2015-01-14

    Abdallah Caramel Bites Recalled for Peanut Contamination

    Abdallah Candies is recalling Holiday Caramel Bites because a customer found a peanut butter bite in the package.

    Product
    Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate (sugar, chocolate liquor, cocoa butter, whole milk, soy lecithin (an emulsifier), vanilla), corn syrup, sweetened condensed milk, cream, sugar, palm oil, salt…
    Category
    Food
    Distribution
    35 states
  • SevereFDA (Devices)·Z-0924-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Remote Controls Due to Unintended Movement

    Trumpf Medical Systems is recalling JUPITER remote controls used with operating tables because complaints were reported of unintended movement during surgical cases.

    Product
    (R)IR remote control JUPITER, Material no.1219656, Serial number: to (incl.) 102317869. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer…
    Category
    Medical Device
    Distribution
    25 states