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.

20801–20825 of 50413

  • HighFDA (Devices)·Z-1267-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Pack Recall for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagent Packs used with Remel M4RT Viral Transport Media due to potential false reactive results.

    Product
    VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent immunoassay intended for the qualitative detection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2021·2021-03-24

    Canon Medical Recalls Catheterization Tables Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because loose bolts may cause the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V207000·2021-03-24

    2021 Thomas Built Buses Saf-T-Liner C2 Recalled for Damaged Valve Stems

    Daimler Trucks North America is recalling 2021 Thomas Built Buses Saf-T-Liner C2 school buses because tire valve stem extensions may be damaged by brake calipers, risking tire pressure loss.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V199000·2021-03-24

    2021 BMW X3 and X4 Fuel Tank Weld May Separate, Increasing Fire Risk

    BMW is recalling certain 2021 X3 and X4 vehicles due to a fuel tank weld that may fail, allowing fuel to leak and increasing fire risk. All repairs have been completed.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1268-2021·2021-03-24

    Carestream Dental CS 3600 Tips Recalled for Detachment Risk

    Carestream Dental is recalling CS 3600 Single Use Normal Tips because the mirror may become detached and fall from the unit.

    Product
    Carestream Dental CS 3600 Single Use Normal Tips, Catalog Number 5941216 - Product Usage: used to record the topographic characteristics of teeth or dental impressions in three dimensions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1275-2021·2021-03-24

    Sirtex Medical Recalls SIROS D-Vial Prep Sets Due to Particulate Matter

    Sirtex Medical Limited is recalling SIROS D-Vial Prep Sets because of a potential presence of particulate matter in the D-Vial.

    Product
    SIROS D-Vial Prep Set, Product Code SIR-10200 - Product Usage: intended for single use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V209000·2021-03-24

    2021 Western Star 4700 and Freightliner Cascadia clutch assembly recall

    Daimler Trucks North America recalls certain 2021 Western Star 4700 and Freightliner Cascadia vehicles because the clutch flange may break, causing clutch disengagement and crash risk. Dealers will replace the clutch assembly free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 interventional angiography systems because the table may tilt if fastening bolts become loose.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1266-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Recalled for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagents because they may produce false reactive results when used with Remel M4RT Viral Transport Media.

    Product
    VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro Diagnostic. The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1251-2021·2021-03-24

    Cardinal Health Recalls McKesson Prevent M Needles Due to Safety Shield Defect

    Cardinal Health is recalling 108,000 McKesson Prevent M needles because the safety shield may fail to lock, posing a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1250-2021·2021-03-24

    Cardinal Health Recalls Magellan Hypodermic Safety Needles Due to Locking Failure

    Cardinal Health is recalling Magellan Hypodermic Safety Needles because the safety shield may fail to lock, creating a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    Magellan Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881850558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21100·2021-03-24

    Flame King Recalls Hog 100-Pound Propane Cylinders Due to Fire Hazard

    Flame King is recalling Hog 100-pound propane cylinders because a manufacturing defect could cause gas leaks and fire. No injuries have been reported.

    Product
    Hog 100-pound Propane Cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21101·2021-03-24

    Beal Birdie Belay Devices Recalled Due to Risk of Climber Injury

    Beal Sas is recalling about 1,400 Birdie Belay Devices because the hand lever can detach, preventing users from lowering climbers. No injuries have been reported.

    Product
    Beal Birdie Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E021000·2021-03-24

    Guangzhou Cougar LED Headlight Bulbs Recalled for Excessive Glare

    Guangzhou Cougar is recalling specific LED headlight bulbs that create excessive glare for oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1252-2021·2021-03-24

    Cardinal Health Recalls Magellan Syringes Due to Safety Shield Defect

    Cardinal Health is recalling Magellan 3 mL syringes with hypodermic safety needles because the safety shield may fail to lock, posing a needlestick risk.

    Product
    Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881833558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V198000·2021-03-22

    Audi Recalls A3 and S3 Models Due to Passenger Air Bag Defect

    Volkswagen Group of America is recalling specific Audi A3 and S3 models because the passenger air bag may deactivate while the seat is occupied.

    Product
    AUDI — AUDI S3, A3, A3 SPORTBACK E-TRON, RS 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-03192021-01·2021-03-19

    USDA Issues Public Health Alert for Uninspected Beef and Lamb Products

    USDA FSIS issued a public health alert for specific beef and lamb products from One Meat Corp. that were produced without federal inspection.

    Product
    FSIS Issues Public Health Alert for Beef and Lamb Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21730·2021-03-18

    Briggs & Stratton Recalls YTL Log Splitters Due to Engine Kickback Injury Hazard

    Briggs & Stratton is recalling YTL log splitters with 250cc engines due to a risk of engine kickback causing injury. Two incidents involving broken wrists have been reported.

    Product
    YTL Log Splitters with Briggs & Stratton 250cc engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V193000·2021-03-18

    2021 Tiffin Phaeton recreational vehicles recalled for loose valve stem

    Tiffin is recalling certain 2021 Phaeton recreational vehicles because the valve stem stabilizer can become loose, allowing the valve stem extender to contact the wheel, which can cause tire pressure loss and increase crash risk.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V188000·2021-03-18

    Chevrolet 2021 Camaro Axle Shaft Separation Defect Recall

    General Motors is recalling certain 2021 Chevrolet Camaro vehicles because the left or right axle shaft may be missing a retaining ring, which could separate during driving and cause loss of power, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V186000·2021-03-17

    2021 Nissan Rogue Incorrect Wheel Nuts May Cause Wheel Separation

    Nissan is recalling certain 2021 Rogue vehicles with incorrect wheel nuts that may loosen and cause wheel vibration. This vibration may break wheel studs and cause wheel separation, increasing crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V184000·2021-03-17

    Jayco Travel Trailers Recalled for Potential Gas Leak Risk

    Jayco is recalling 2019-2020 travel trailers because a stove component may cause a gas leak, increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK, JAY FEATHER, JAY FLIGHT SLX, JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide