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.

39101–39125 of 50506

  • HighFDA (Food)·F-1978-2015·2015-04-22

    Culinary Masters Steak Dust Spice Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Steak Dust Fulton's Spice because cumin used in the product contained undeclared peanuts.

    Product
    Culinary Masters, STEAK DUST FULTONS SPICE, Pack Size 50 LB
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1453-2015·2015-04-22

    US Endoscopy Recalls Talon Grasping Devices Due to Detached Wire Component

    US Endoscopy Group Inc is recalling 1,695 Talon Grasping Devices because a wire component on the distal grasping assembly became detached.

    Product
    Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    42 states
  • HighCPSC·15120·2015-04-22

    Shark Vacuum Cleaners Recalled by Euro-Pro Due to Shock Hazard

    Euro-Pro is recalling Shark vacuum cleaners because the aluminum wand can disconnect and remain energized, posing an electric shock risk.

    Product
    Shark Powered Rotator Lift-Away vacuum cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1954-2015·2015-04-22

    ProThera Recalls Ther-Biotic Probiotic Supplements Due to Glass Shards

    ProThera, Inc. is recalling three lots of Ther-Biotic Children's Chewable probiotic supplements because shards of blue glass were found in the bottles.

    Product
    Klaire Labs Ther-Biotic Children's Chewable 125+ Billion CFU's Multi-Species Probiotic Supplement 60 Chewable Capsules. UPC 7 09616 01247 5 Manufactured by ProThera Inc . Klaire Labs is a division of ProThera, Reno, NV.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1979-2015·2015-04-22

    Culinary Masters BBQ Spice Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters BBQ spice because cumin ingredients contained undeclared peanuts.

    Product
    Culinary Masters, SPICE FULTONS BBQ, Net Wt. 50 LB, Distributed by Gourmet Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1966-2015·2015-04-22

    Whole Foods Salted Caramel Crispies Cookies Recalled for Undeclared Almonds

    Whole Food Market is recalling Salted Caramel Crispies Cookies because they contain undeclared almonds, posing a risk to individuals with allergies.

    Product
    Whole Foods Salted Caramel Crispies Cookies, 12 pack packaged in cellophane with tie closure
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1447-2015·2015-04-22

    Bard Monopty Disposable Core Biopsy Instruments Recalled for Activation Issues

    Bard Peripheral Vascular is recalling specific Bard Monopty Disposable Core Biopsy Instruments and Kits due to potential activation-related issues.

    Product
    Bard Monopty Disposable Core Biopsy Instruments and Kits, Monopty 14g x 16cm (22mm), Product Code: 121416; Monopty Biopsy, Product Code: 000441; Monopty 14g x 10cm (22mm), Product Code: 121410; Monopty 14g x 10cm (11mm), Product Code: 211410. The BARD MONOPTY Disposable Core…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1953-2015·2015-04-22

    ProThera Recalls Ther-Biotic Probiotic Supplements Due to Glass Shards

    ProThera, Inc. is recalling specific lots of Klaire Labs Ther-Biotic FACTOR 6 probiotic supplements because blue glass shards were found in the bottles.

    Product
    Klaire Labs Ther-Biotic FACTOR 6 100+ Billion CFU's Multi-Species Probiotic Supplement 60 Vegetarian Capsules. UPC 7 09616 01248 2 Manufactured by ProThera Inc . Klaire Labs is a division of ProThera, Reno, NV.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1976-2015·2015-04-22

    Culinary Masters Pork Paprika Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters SPICE BLEND PORK PAPRIKA because cumin ingredients contained undeclared peanuts.

    Product
    Culinary Masters, SPICE BLEND PORK PAPRIKA, Net Wt. 30 lbs., Distributed by Gourmet Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1450-2015·2015-04-22

    CooperSurgical Recalls Wallach LL 100 Cryosurgical Units Due to Gas Line Burst Risk

    CooperSurgical is recalling 255 Wallach LL 100 cryosurgical units because an internal gas line may malfunction and burst under pressure.

    Product
    WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number 900019-70; LL100 Multi Tip W/TC - Part Number: 900629; LL100 - CO2 - Part Number 900162
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2015·2015-04-22

    Bard ConQuest PTA Balloon Dilatation Catheter Recalled for Deflation Risk

    Bard Peripheral Vascular is recalling specific lots of the ConQuest PTA Balloon Dilatation Catheter due to a risk of deflation-related issues.

    Product
    Bard ConQuest PTA Balloon Dilatation Catheter, 12mm Balloon Size, Product Code: CQ-75124.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1952-2015·2015-04-22

    Twin Tree Gardens Chicken Rub Recalled for Undeclared Peanut Allergen

    Haddon House Food Products is recalling Twin Tree Gardens Chicken Rub because it may contain undeclared peanut allergen.

    Product
    Twin Tree Gardens Premium Rubs "bunkhouse" Chicken Rub, Net Wt. 2.75 oz. (77g), Distributed by: Flavor Delight, Inc., Richburg, South Carolina, UPC 041278582362
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1946-2015·2015-04-22

    PureLife Naturals Multi-Action Immunity Recalled for Gluten Mislabeling

    ReNew Life Formulas is recalling PureLife Naturals Multi-Action Immunity supplements because labels claim 'no wheat' and 'no gluten' but the products contain gluten or wheat-related allergens.

    Product
    PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle
    Category
    Food
    Distribution
    51 states
  • HighFDA (Food)·F-1988-2015·2015-04-22

    Culinary Masters Cajun Steak Seasoning Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Cajun Steak Seasoning Blend because the cumin used in the product contains undeclared peanuts.

    Product
    Culinary Masters, MASTERS CAJUN STEAK SEASONING BLEND, Net Wt. 20 oz. and 7 lbs, Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1955-2015·2015-04-22

    Kraft Macaroni and Cheese Recalled for Potential Metal Contamination

    Kraft Foods Group Inc. is voluntarily recalling boxed Macaroni & Cheese dinners because they may contain metal pieces.

    Product
    Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four different package types affected by this recall: 1) single 7.25 oz boxes, 3-pack box of 7.25 oz boxes, 4-pack shrink wrap of 7.25 oz boxes, and 5-pack shrink…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15119·2015-04-21

    AG Hair Sweet Heat Hair Dryers Recalled for Electrocution Hazard

    AG Hair is recalling about 3,100 Sweet Heat hair dryers because they lack an immersion protection device, posing an electrocution risk if submerged in water.

    Product
    Sweet Heat Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V236000·2015-04-21

    Toyota Recalls 2015 Siennas for Potential Trim Panel Detachment Risk

    Toyota is recalling 2015 Siennas with dealer-installed entertainment systems because a reused clip may allow a trim panel to detach during airbag deployment.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15116·2015-04-21

    Gorsuch Recalls Ertlrenz Ski Boot Heat Liners Due to Fire Hazard

    Gorsuch is recalling Ertlrenz ski boot heat liners because they can overheat while charging, posing a fire hazard. No injuries have been reported.

    Product
    Ertlrenz Trim Heat and Foam Heat ski boot liners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V237000·2015-04-21

    Coachmen Freelander and Leprechaun Recalled for Incorrect Weight Labels

    Forest River is recalling 2015-2016 Coachmen Freelander and 2015 Leprechaun vehicles because incorrect weight labels may lead to overloading and increased crash risk.

    Product
    COACHMEN — COACHMEN FREELANDER, LEPRECHAUN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E030000·2015-04-20

    Cummins Westport ISL G Engine Recall for Fire Risk

    Cummins is recalling Westport ISL G engines because excessive crankcase pressure may cause a vent tube to detach, allowing oil to contact hot surfaces and increase fire risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V233000·2015-04-20

    Mitsubishi Recalls Lancer and Outlander Models for Blower Motor Defect

    Mitsubishi is recalling 76,958 vehicles because a blower motor failure may reduce windshield defroster performance, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER SPORTBACK, OUTLANDER SPORT, LANCER EVOLUTION, LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V232000·2015-04-20

    Mitsubishi Recalls Lancer and Outlander Models for Electrical Control Unit Defect

    Mitsubishi is recalling certain 2009-2010 Lancer, Outlander, Lancer Sportback, and Lancer Evolution vehicles because an unstable voltage in the electronic control unit may cause lights and wipers to fail, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER, OUTLANDER, LANCER EVOLUTION, LANCER SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V229000·2015-04-17

    Volkswagen and Audi Recall 2015 Models for Fuel Pump Defect

    Volkswagen Group of America is recalling 2015 Golf, GTI, and Audi A3 vehicles because a fuel pump defect may cause the engine to stall, increasing crash risk.

    Product
    AUDI — AUDI, VOLKSWAGEN A3 CABRIOLET, GOLF, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide