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.

18226–18250 of 50404

  • HighNHTSA·22V031000·2022-01-25

    Kia Recalls Vehicles Due to Potential Air Bag Deactivation

    Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.

    Product
    KIA — KIA FORTE KOUP, SOUL EV, SEDONA, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V027000·2022-01-24

    2022 Mitsubishi Outlander Recalled for Defective Fuel Pump

    Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V022000·2022-01-21

    Kia Recalls 2020 Cadenza for Rear Power Window Safety Issue

    Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V026000·2022-01-21

    Trails West Recalls 2017-2021 Trailers Due to Propane Regulator Fire Risk

    Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST SIERRA, FREERIDE, CLASSIC, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V018000·2022-01-20

    2021-2022 Heartland RVs Recalled for Tire Belt Separation Risk

    Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.

    Product
    HEARTLAND — HEARTLAND CYCLONE, GRAVITY, FUEL, ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0391-2022·2022-01-19

    Classic Lasagna Pasta Sheets Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Classic Lasagna Pasta sheets because the label declares flour as an ingredient but fails to declare wheat, which is present in the product. Consumers with wheat allergies may face serious health risks.

    Product
    Classic Lasagna Pasta sheets sold frozen and wrapped in brown freezer paper. The weight per package is 1 lb/453.6 grams. The label is read in parts: "***Classic Lasagna sheets *** Ingredients: Flour, Semolina, Egg, water ***www.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0476-2022·2022-01-19

    Philips wireless footswitches for Allura Xper and Azurion X-ray systems recalled for connection issues

    Philips wireless footswitches used with Allura Xper and Azurion X-ray systems may experience connection issues that interrupt fluoroscopic imaging during patient procedures. The recall affects 1,971 systems distributed worldwide.

    Product
    Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number: 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0381-2022·2022-01-19

    Bosket Bread Sourdough Bread Lacks Required Ingredient Statement

    Bosket Bread Company is recalling sourdough bread products sold in Washington because packages are missing required ingredient statements, leaving consumers unable to identify potential allergens including wheat, milk, egg, soy, and sesame.

    Product
    Sourdough 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
  • HighFDA (Devices)·Z-0466-2022·2022-01-19

    Proton Therapy System software startup allows test processes to contaminate clinical environment

    The Proteus 235 proton therapy system can start clinical processes while test processes are still running, potentially using test components in clinical treatments without user notification. This could impact patient treatment if versions differ.

    Product
    Proteus 235; Version: PTS-8 versions before PTS-8.7.2
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0491-2022·2022-01-19

    Medtronic Perfusion Kits Recalled: Missing Endotoxin Testing

    Medtronic is recalling approximately 6,653 Custom Perfusion kits used in cardiac procedures because they were labeled as non-pyrogenic without completing required endotoxin testing.

    Product
    Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R FILTER (Model BB10Q85R); 2. CUSTOM PACK BB11C01R MIDI DEEP (Model BB11C01R); 3. CUSTOM PACK BB7H95R22 HYP MAIN (Model B7H95R22)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0474-2022·2022-01-19

    Computed Tomography System Software May Degrade Head Image Quality

    Siemens SOMATOM Edge Plus CT systems running software version VB20_SP5 may produce degraded head images, potentially leading to patient misdiagnosis.

    Product
    SOMATOM Edge Plus-Computed tomography system Model 1026700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0389-2022·2022-01-19

    Pie Dough Recall: Undeclared Wheat Allergen

    Local Fixe LLC is recalling frozen pie dough products because wheat is not declared on the label, even though flour—which contains wheat—is an ingredient. The recall affects 181 packages distributed in Oregon.

    Product
    Pie Dough are packaged two crusts per pack and sold frozen. They are wrapped in white butcher paper. The weight per package is 1.257 lbs/540 grams. The label is read in parts: "***Pie Dough*** Flour, Butter (cream, milk, salt), Organic Palm Shortening, water, salt…
    Category
    Food
    Distribution
    1 state
  • HighCPSC·22054·2022-01-19

    FRIGG Silicone Pacifiers Recalled Due to Choking Hazard

    Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.

    Product
    FRIGG Silicone Pacifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0395-2022·2022-01-19

    Vemondo Vegan Dessert Cones Recalled for Undeclared Milk Allergen

    Lidl US Operations is recalling Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones because they contain undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones. 4-3.7 fl oz (110 mL) UPC 4 056489 468653
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0477-2022·2022-01-19

    OCT-Camera Laser Shut-Off Malfunction Poses Patient Safety Risk

    Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.

    Product
    OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22055·2022-01-19

    Children's Sleepwear Recalled for Flammability Standards Violation

    Childrensalon is recalling about 180 children's sleepwear garments that fail to meet U.S. flammability standards, posing a burn injury risk. Consumers should stop using the garments immediately and contact Childrensalon for return instructions.

    Product
    Children's Sleepwear Garments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0369-2022·2022-01-19

    Bosket Bread Sourdough Dinner Rolls Lack Required Ingredient Labels

    Bosket Bread Company is recalling Sourdough Dinner Rolls distributed in Washington because the products lack ingredient statements, leaving consumers unable to identify undeclared wheat, milk, egg, soy, or sesame allergens.

    Product
    Sourdough Dinner 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-0388-2022·2022-01-19

    Fresh Flour Tortillas Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Fresh Flour Tortillas because wheat is not declared on the label, even though flour (a wheat product) is listed as an ingredient. This poses a risk to consumers with wheat allergies.

    Product
    Fresh Flour Tortillas are packaged in a clear Ziploc style plastic bag. The weight per package is 1.323 lbs/600 grams. The label is read in parts: "***Fresh Flour Tortillas ***Flour, water, organic palm shortening, salt, baking powder*** ww.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0380-2022·2022-01-19

    Bosket Bread Sesame Buns Recalled for Undeclared Allergens

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

    Product
    Sesame Buns, 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 (Devices)·Z-0472-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality Nationwide

    Siemens SOMATOM Confidence CT scanners with software version VB20_SP5 may experience degraded head image quality, creating a potential risk of misdiagnosis. The recall affects 108 units distributed nationwide.

    Product
    SOMATOM Confidence -Computed tomography systems Model 10590100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0492-2022·2022-01-19

    Flat Panel Detector May Display Abnormal Images During Surgical Procedures

    Canon Medical's flat panel detectors used in Alphenix surgical systems may display abnormal horizontal stripes and fail to recover by restarting, potentially causing operators to work without proper visual guidance during procedures.

    Product
    Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C, INFX-8000F, and INFX-8000H.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0484-2022·2022-01-19

    GLOBAL UNITE STD STEM orthopedic implant manufacturing defect recall

    DePuy Orthopaedics is recalling GLOBAL UNITE STD STEM orthopedic implants due to undersized spigot bore diameter that may prevent proper removal during revision surgery, risking surgical delay and bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0379-2022·2022-01-19

    Bosket Bread Olive Bread recalled for undeclared allergens

    Bosket Bread Company is recalling Olive Bread (Kalamata olives) products distributed in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Olive Bread (Kalamata olives), 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-0370-2022·2022-01-19

    Bosket Bread Rosemary Bread recalled for undeclared allergens

    Bosket Bread Company is recalling Rosemary Bread products sold in Washington due to missing ingredient statements, which fail to declare potential wheat, milk, egg, soy, or sesame allergens.

    Product
    Rosemary 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