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.

20826–20850 of 50413

  • HighFDA (Devices)·Z-1179-2021·2021-03-17

    Draeger VentStar Watertrap Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 150 units of VentStar Watertrap (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2021·2021-03-17

    Canon Medical System INFX-8000C C-Arm Recall for X-Ray Field Shift

    Canon Medical System is recalling 272 INFX-8000C C-arm systems nationwide because the x-ray irradiation field may shift relative to the displayed image at certain angles.

    Product
    System INFX-8000C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1180-2021·2021-03-17

    Dräger ID Circuit Basic Breathing Circuits Recalled for Detachment Risk

    Dräger Medical is recalling ID Circuit Basic (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2021·2021-03-17

    Sunstar G.U.M. Hydral Dry Mouth Spray Recalled for Bacterial Contamination

    Sunstar Americas is recalling 56,960 bottles of G.U.M. Hydral Dry Mouth Relief Oral Spray due to potential Burkholderia cepacia contamination.

    Product
    SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2021·2021-03-17

    Insulet Recalls Omnipod DASH User Guides Due to Decimal Error

    Insulet Corporation is recalling 21,723 Omnipod DASH User Guides distributed outside the US due to a misprint regarding decimal separators that could lead to incorrect bolus delivery.

    Product
    Omnipod DASH Insulin Management System User Guide (OUS Only) Product Catalog Number: PT 000002 XXX XXX XX PT 000318 PT 000319 Distributed to: Canada (French only), the Netherlands, France, Austria, Germany, Belgium, Greece, Turkey, Norway, Sweden, Denmark, and Finland
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1186-2021·2021-03-17

    Stryker Recalls Triathlon Knee Baseplates Due to Manufacturing Defect

    Stryker is recalling 11 Triathlon Tritanium Tibial Baseplates because a manufacturing defect may prevent the knee insert from locking securely.

    Product
    Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-1181-2021·2021-03-17

    Getinge Flow i Anesthesia Systems Recalled for Absorber Docking Failures

    Getinge Group Logistics America is recalling 144 Flow i Anesthesia Systems due to complaints of incorrect FiCO2 readings and System Check Out failures when docking the absorber.

    Product
    Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2021·2021-03-17

    Westminster Cracker Inc. Recalls Oyster Crackers Due to Plastic Foreign Object

    Westminster Cracker Inc. is recalling specific oyster cracker products because they may contain hard plastic foreign objects. Consumers should check their pantries for the affected items.

    Product
    Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 12 per case - UPC 093215200426; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 6 per case - UPC 093215200426
    Category
    Food
    Distribution
    13 states
  • HighCPSC·21097·2021-03-17

    HOFISH Recalls Mattresses for Federal Flammability Standard Violation

    HOFISH is recalling 10-inch hybrid mattresses sold on Amazon.com because they fail to meet the mandatory federal flammability standard, posing a fire hazard.

    Product
    HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V185000·2021-03-17

    2021 Hyundai Santa Fe Air Bag Child Detection System Defect

    2021 Hyundai Santa Fe vehicles have a defective Occupant Detection System that may fail to prevent air bag deployment when a child restraint is detected in the front passenger seat, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1202-2021·2021-03-17

    Thermo Fisher Recalls Cascadion Clinical Analyzer Due to Software Defect

    Thermo Fisher Scientific is recalling 19 Cascadion Clinical Analyzers because a software defect may cause false Vitamin D deficiency results.

    Product
    Cascadion SM Clinical Analyzer, REF 99990000 SN Type: 9910
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1178-2021·2021-03-17

    Dräger VentStar Basic Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 1,525 VentStar Basic breathing circuits because a Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0337-2021·2021-03-17

    Hu Chocolate-Covered Hunks Recalled for Undeclared Almonds

    Hu Products LLC is recalling Chocolate-Covered Hunks Sour Goldenberries because the product may contain undeclared almonds.

    Product
    Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g); packaged in a black bag; Distributed by: Hu Products LLC, NY, NY 10011
    Category
    Food
    Distribution
    8 states
  • HighNHTSA·21V178000·2021-03-16

    2021 Keystone Cougar Trailers Recalled for Electrical Shock Hazard in Inverter

    Certain 2021 Keystone Cougar trailers equipped with the Off the Grid Solar package may have an incorrectly wired inverter that energizes the shore power connection, posing an electrical shock risk. Keystone will repair the inverter at no charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V176000·2021-03-15

    2021 BMW 430i and M440i side-thorax airbags may fail to deploy

    2021 BMW 430i and M440i models have defective side-thorax airbags that may not deploy during side-impact crashes, increasing injury risk. Owners should contact their dealer for a free software update.

    Product
    BMW — BMW M440I, 430I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V177000·2021-03-15

    Ditch Witch Trailers Recalled for Missing Side Reflectors

    Charles Machine Works is recalling specific Ditch Witch trailers because they may be missing side reflex reflectors, which reduces visibility to other drivers.

    Product
    DITCH WITCH — DITCH WITCH ZS6S, S4S, 745-7900, 025-1020
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V172000·2021-03-12

    2021 Coachmen Viking Travel Trailers Cooktop Fire Risk Recall

    Forest River, Inc. is recalling certain 2021 Coachmen Viking and Clipper travel trailers because the cooktop may not be properly isolated from the furnace return air, which can cause the flame to invert and increase fire risk. Dealers will install and seal a panel free of charge.

    Product
    COACHMEN — COACHMEN CLIPPER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-03122021-01·2021-03-12

    Vons Chicken Noodle Soup Recalled for Incorrect Gluten-Free Labeling

    USDA FSIS issued a public health alert for Vons Signature CAFÉ Chicken Noodle Soup due to misbranding. The product is labeled gluten-free but contains wheat, posing a risk to consumers with gluten allergies.

    Product
    The Vons Companies, Inc. — FSIS Issues Public Health Alert for Chicken Soup Product Due to Misbranding
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·21V171000·2021-03-12

    ATC Recalls 2018-2021 ARV Trailers Due to Insufficient Safety Chains

    ATC is recalling 2018-2021 ARV Gamechanger and Pro Bumper Pull trailers because the installed safety chains are rated lower than the trailer's axle capacity, posing a crash risk.

    Product
    ATC ARV — ATC ARV PRO BUMPER PULL, GAMECHANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V163000·2021-03-11

    2021 RAM Cummins Diesel Cab Chassis Trucks Recalled for Electrical Fire Risk

    Chrysler is recalling approximately 19,214 2021 RAM heavy-duty trucks with diesel engines due to a potential electrical short in the intake heater relay that could cause vehicle fires. Owners should not park these vehicles indoors until repaired.

    Product
    RAM — RAM 5500, 2500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V164000·2021-03-11

    2021 Kia K5 Air Bag Detection System Recall for Child Restraint Safety

    Kia is recalling certain 2021 K5 vehicles because the occupant detection system may fail to recognize child restraints, risking air bag deployment during a crash.

    Product
    KIA — KIA K5, FORTE, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide