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.

18276–18300 of 50406

  • HighFDA (Food)·F-0394-2022·2022-01-19

    Vemondo Vegan Coconut & Cocoa Dessert Cones Recall for Undeclared Milk

    Lidl US Operations is recalling Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones due to undeclared milk allergen. The product was distributed to retail stores in Maryland, Virginia, and Pennsylvania.

    Product
    Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0374-2022·2022-01-19

    Bosket Bread Country Loaf recalled for undeclared allergens

    Bosket Bread Company is recalling Country Loaf bread products distributed in Washington because packages lack ingredient statements, creating risk of undeclared wheat, milk, egg, soy, or sesame exposure.

    Product
    Country Loaf, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0373-2022·2022-01-19

    Bosket Bread Cinnamon Rolls recalled for undeclared allergens

    Bosket Bread Company is recalling cinnamon rolls (1–1.5 lbs, packaged in plastic bags) distributed in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Cinnamon Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0368-2022·2022-01-19

    Bosket Bread Baguettes Recalled for Undeclared Allergens

    Bosket Bread Company is recalling baguettes distributed in Washington due to missing ingredient statements on packaging. The products may contain undeclared wheat, milk, egg, soy, or sesame.

    Product
    Baguettes, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Bread is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0392-2022·2022-01-19

    Local Fixe LLC Soup Noodles Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Soup Noodles because wheat is not declared on the label despite flour (a wheat-containing ingredient) being present in the product. Consumers with wheat allergies may face serious health risks.

    Product
    Soup Noodles are raw pasta cut into assorted rectangle shapes and sold frozen. Product is packaged in clear half quart plastic Ziploc style bags and then wrapped in brown freezer paper. The weight per package is 8 oz/227 grams. The ingredients are read in parts: "***Soup…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0469-2022·2022-01-19

    Sterilized medical convenience kits recalled for missing latex warning label

    ROi CPS LLC is recalling 195 Regard T AND A - Rogers sterilized convenience kits due to missing rubber latex warning labels. Consumers with latex allergies face risk of allergic reaction if exposed to the unlabeled latex.

    Product
    Regard, T AND A - Rogers, sterilized convenience kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0396-2022·2022-01-19

    Chili & Cheese Brat on Pretzel Bun Recalled for Undercooked Sausage

    Kitchen Fresh Foods is recalling Chili & Cheese Brat on Pretzel Bun products because the sausage was not fully cooked. The recall affects 1,069 pieces distributed across multiple states.

    Product
    Chili & Cheese Brat on Pretzel Bun, Item Number 1098, Net Wt. 6.5 oz(185g), UPC 7 47804-01098 8. Keep Refrigerated. Packaged under the following brands: 1. Grabn'Go, MFG BY: KF Foods, Green Bay, WI 54313; 2. Fox River Vending Inc. Dst By: Fox River Appleton WI…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0490-2022·2022-01-19

    Hip prosthetic stem undersized bore complicates removal surgery

    DePuy Orthopaedics' GLOBAL UNITE STD STEM prosthetics may have undersized spigot bores, complicating removal during revision surgery. Affected patients may experience surgical delays or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0489-2022·2022-01-19

    Hip Stem Device Recalled Due to Undersized Bore Diameter Risk

    DePuy Orthopaedics recalls the GLOBAL UNITE STD STEM SZ 14 hip stem in 451 units worldwide due to undersized spigot bore diameter. The defect may prevent proper separation of the stem during surgery without surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0470-2022·2022-01-19

    RefleXion Medical Radiotherapy System Recall Due to Dose Discrepancy

    Reflexion Medical is recalling three RefleXion X1 radiotherapy systems due to a potential dose discrepancy when delivering treatment in Feet First Supine patient orientation.

    Product
    RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: "RefleXion X1 Model: RXM1000"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2022·2022-01-19

    Philips Azurion X-ray System recalled for startup and emergency stop failures

    Philips recalls 10 Azurion interventional X-ray systems due to intermittent startup communication failures and emergency stop recovery issues that could prevent system restart and movement functionality.

    Product
    Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration start-up issue; Azurion R2.2 emergency stop recovery issue Model Numbers: 722221, 722228, 722225, 722068, 722226, 722078, 722224
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0372-2022·2022-01-19

    Bosket Bread Cinnamon Bread Recall for Undeclared Allergens

    Bosket Bread Company is recalling Cinnamon Bread products distributed in Washington because the packages lack ingredient statements, making it impossible for consumers to identify potential allergens including wheat, milk, egg, soy, and sesame.

    Product
    Cinnamon Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V017000·2022-01-19

    Dennis Eagle Elite and Proview Recalled for Window Malfunction

    Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because windows may not open or close properly, potentially distracting drivers.

    Product
    DENNIS EAGLE — DENNIS EAGLE ELITE, PROVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V016000·2022-01-18

    2022 Peterbilt 579 chassis step bolts may loosen and cause injury

    Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V015000·2022-01-17

    2022 Keystone Alpine RV Exterior Ladder May Detach from Rear Wall

    Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.

    Product
    KEYSTONE — KEYSTONE ALPINE, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V013000·2022-01-14

    2021 Ford Diesel Trucks Fuel Filter Cap Defect Fire Risk

    Ford is recalling certain 2021 diesel trucks due to a void in the secondary fuel filter cap that may leak fuel, posing a fire risk. Dealers will replace the fuel filters free of charge.

    Product
    FORD — FORD F-550 SD, F-450 SD, F-650, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V012000·2022-01-14

    2022 Forest River Cherokee toy hauler tires may be incorrectly specified on placard

    Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V010000·2022-01-13

    Seagrave Recalls 2011-2021 Firetrucks Due to Cracking Crossmember Plate

    Seagrave is recalling 2011-2021 Marauder and Capitol firetrucks because a crossmember mounting plate may crack, potentially distracting the driver and increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2022·2022-01-12

    COVID-19 Diagnostic Kit Recall for Inaccurate Test Results

    Qiagen Sciences is recalling 376 units of its QIAstat-Dx Respiratory SARS-CoV-2 Panel diagnostic kit due to faulty cartridges that can produce false-negative or false-positive test results.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0445-2022·2022-01-12

    Power wheelchairs with LiNX Gyro module recalled for deceleration control failure

    Invacare power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, risking user injury due to an incorrect deceleration profile.

    Product
    Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, TDXSP2HD-MCG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22052·2022-01-12

    EGL and ACE Youth All-Terrain Vehicles Recalled for Safety Standard Violations

    EGL Motor is recalling about 2,900 EGL and ACE branded youth ATVs (models MADIX 125 and D110) because they fail federal safety standards, allowing children to exceed safe speeds and creating laceration and crash hazards.

    Product
    EGL and ACE Branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2022·2022-01-12

    Medical Device Kit Poses Risk of Sample Leakage and Lab Contamination

    DiaSorin Molecular's Simplexa Direct Amplification Disc Kit is recalled due to risk of leakage when used multiple times, which may cause cross-contamination in laboratory settings if not properly cleaned.

    Product
    Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-0462-2022·2022-01-12

    Alinity m System recalled for software defect in amplification detection

    Abbott Molecular is recalling 742 Alinity m Systems worldwide due to a software defect that can set the Amplification Detection clamp CLEAN position too high, potentially affecting instrument operation.

    Product
    Alinity m System, Part No. 08N53-002
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0463-2022·2022-01-12

    Abbott Alinity m System camera firmware installation issue

    Abbott Molecular is recalling 74 Alinity m Systems due to an issue with the installation of updated camera firmware. Affected devices were distributed in the United States and internationally.

    Product
    Alinity m System, Part No. 08N53-002
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-0365-2022·2022-01-12

    Trader Joe's Soycutash recalled for Listeria contamination

    Trader Joe's Soycutash (Item #99319), a frozen mix of sweet corn, shelled edamame, and red bell peppers, is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in Arizona, California, Nevada, and Utah.

    Product
    Trader Joe's Soycutash, Item # 99319. A mix of Sweet Corn, Shelled Edamame, and Red Bell Peppers. Net Wt. 16 oz. (1 lb.) 454g. Keep Frozen. UPC 0099-3197. Dist & Sold Exclusively By: Trader Joe's Monrovia, CA 91016
    Category
    Food
    Distribution
    4 states