The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

38751–38775 of 50506

  • HighFDA (Food)·F-2280-2015·2015-05-20

    Gourmet Kitchen Recalls Lobster and Shrimp Spring Rolls for Peanut Allergen

    Gourmet Kitchen, Inc. is recalling Lobster & Shrimp Spring Rolls because they may contain peanut protein. The recall covers 120 boxes distributed nationwide.

    Product
    Lobster & Shrimp Spring Rolls Products are placed on plastic trays, shrink wrapped, placed in boxes, labelled, & shrink wrapped.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15138·2015-05-19

    Precision Trading Recalls Espresso Makers Due to Burn Risk

    Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.

    Product
    PREMIUM® Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15139·2015-05-19

    Kaldi's Coffee Recalls Disposable Cup Sleeves Due to Fire Hazard

    Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.

    Product
    Disposable Cup Sleeves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V295000·2015-05-19

    Gillig Low Floor Bus Taillight Bracket Recall

    Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V292000·2015-05-18

    New Flyer Buses Recalled for Engine Vent Tube Fire Risk

    New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V291000·2015-05-18

    Fiat 500 Electric Recall for Transmission Shifting to Neutral

    Chrysler is recalling 2013-2015 Fiat 500 electric vehicles because a software issue may cause the transmission to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·078-2015·2015-05-16

    A.S.K. Foods Recalls Herb Stuffing Due to Undeclared Soy Allergen

    A.S.K. Foods is recalling 414 pounds of Wegmans Herb Stuffing with Pork and Veal because the product contains undeclared soy lecithin.

    Product
    A.S.K. Foods Inc. — A.S.K. Foods, Inc. Recalls Herb Stuffing with Pork and Veal Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1574-2015·2015-05-13

    MHI-TM2000 Linear Accelerator System Software Recall for Communication Errors

    Mitsubishi Heavy Industries is recalling 11 MHI-TM2000 Linear Accelerator Systems due to a software defect that allows radiation delivery despite communication errors and prevents saving treatment records.

    Product
    MHI-TM2000 Linear Accelerator System (Software Version 3.5.0 and 3.5.1)
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1586-2015·2015-05-13

    Bard MAX-CORE Biopsy Instruments Recalled for Self-Activation Risk

    Bard Peripheral Vascular Inc is recalling 7,995 Bard MAX-CORE Disposable Core Biopsy Instruments due to a risk of self-activation-related issues.

    Product
    BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g x 20cm The BARD MAX-CORE Disposable Core Biopsy Instrument is a single patient use core biopsy device. It is available in several needle gauge sizes and lengths. The side and rear actuator buttons are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2155-2015·2015-05-13

    Spiceco Recalls Emeril's Blackened Seasoning Blend for Undeclared Peanut

    Spiceco is recalling Emeril's Blackened Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,483 cases distributed nationwide and abroad.

    Product
    Emeril's Blackened Seasoning Blend, 3.1 oz. (88g) Distributed by: B&G Foods, Inc., Parsippany, NJ 07054 USA, UPC 074683097633
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2015·2015-05-13

    Spacelabs Ultraview SL Command Modules Recalled for Random Resets

    Spacelabs is recalling Ultraview SL Command Modules with specific Masimo SpO2 components due to a defect causing random resets.

    Product
    Ultraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an adult or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2015·2015-05-13

    Stryker Recalls Ambulating Bulbs Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling Ambulating Bulbs used with wound drains because of a potential sterility breach in the packaging.

    Product
    Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main components: the suction reservoir, the PVC tubing, the slide clamp and the female connector. The rigid polycarbonate female connector is used to connect the ambulating bulb to the CBCII evacuator tube in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2193-2015·2015-05-13

    Whole Foods Market Rye Bread Recalled for Undeclared Wheat

    Whole Foods Market is recalling Health Starts Here Rye Bread in Texas, Oklahoma, Arkansas, and Louisiana due to undeclared wheat.

    Product
    Whole Foods Market Health Starts Here Rye Bread (formerly 100% Rye) 16 oz. PLU# 41844
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1593-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Potential Leakage

    ICU Medical is recalling 5,100 units of MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    127" (323cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33351 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2175-2015·2015-05-13

    Cott Beverages Recalls Red Rain Energy Drink for Unlabeled Tree Nuts

    Cott Beverages is recalling Red Rain Energy Drink Tropical Mango because it may contain trace amounts of walnuts, a tree nut not listed on the ingredient label.

    Product
    Red Rain Energy Drink Tropical Mango
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2166-2015·2015-05-13

    Spiceco Recalls Fish Rub Seasoning for Undeclared Peanut Protein

    Spiceco is recalling Pride of Szeged Fish Rub Seasoning because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Pride of Szeged Fish Rub Seasoning Net Wt. 5 oz (142 g) Spiceco, Avenel NJ 07001 UPC 078006020018 2.75 oz 50 lb boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2156-2015·2015-05-13

    Spiceco Recalls Sylvia's Rib Rub N More Seasoning for Undeclared Peanut

    Spiceco, Inc. is recalling Sylvia's Rib Rub N More Seasoning because it may contain undeclared peanut protein. The recall includes 324 cases distributed nationwide and abroad.

    Product
    Sylvia's Rib Rub N More Seasoning, Net Wt. 5.5 oz. (155g), Distributed by: Sylvia Woods Food Company, P.O. Box 240, Harlem, NY 10027, UPC 608623000683
    Category
    Food
    Distribution
    Distributed nationwide