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.

39626–39650 of 50506

  • HighFDA (Devices)·Z-1053-2015·2015-02-11

    CareFusion Recalls SmartSite Infusion Sets Due to Disconnection and Leakage

    CareFusion is recalling 7,440 SmartSite Low Sorbing Infusion Sets due to disconnection and leakage issues.

    Product
    SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. The set is comprised of components commonly found on intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15076·2015-02-10

    Marin Recalls 2014 MBX 50 and Tiny Trail Children's Bicycles

    Marin Mountain Bikes is recalling 2014 MBX 50 and Tiny Trail children's bicycles because handlebars can loosen or separate, posing a crash and injury risk.

    Product
    2014 Marin MBX 50 and Tiny Trail Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V080000·2015-02-10

    Forest River Recalls 2014 Rockwood and Flagstaff RVs for Fire Risk

    Forest River is recalling 726 model year 2014 Rockwood and Flagstaff recreational vehicles equipped with the Chill Chaser option due to a fire risk from loose wiring or foam insulation contacting the heating element.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V076000·2015-02-09

    Nova Bus Recalls 2008 LFS Transit Buses for Emergency Exit Defect

    Nova Bus is recalling 2008 LFS transit buses because surrounding material may interfere with opening emergency exit windows, increasing injury risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V078000·2015-02-09

    Nova Bus Recalls 2009 LFS Transit Buses Due to Wiring Defect

    Nova Bus is recalling 2009 LFS transit buses because an incorrectly wired main power relay circuit may defeat circuit protection, increasing the risk of fire.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V070000·2015-02-06

    Altec Recalls 2005-2013 Crane Telescopic Jibs Due to Pin Placement Risk

    Altec is recalling 724 crane telescopic jibs from 2005-2013 because the limiting pin may not be inserted correctly, allowing unimpeded movement that could injure operators or nearby individuals.

    Product
    ALTEC — ALTEC CRANE TELESCOPIC JIB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V068000·2015-02-06

    OBS Recalls School Buses with Cracking Wheelchair Lifts

    OBS is recalling certain school buses equipped with Ricon wheelchair lifts where the platform side plate may crack, posing an injury risk to operators.

    Product
    COLLINS — COLLINS, BLUE BIRD, OBS MIDSTAR 20IS, A3FE2803A, CHEVY CG33803, BBCV3011S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15T003000·2015-02-06

    Toyo Open Country M/T Tires Recalled for Tread Separation Risk

    Toyo is recalling specific Open Country M/T tires due to off-center belts that may cause tread separation or loss of inflation pressure, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15073·2015-02-05

    Sea Gull Lighting Recalls Chandeliers Due to Falling Hazard

    Sea Gull Lighting is recalling about 8,800 chandeliers in the U.S. and 800 in Canada because the screw collar can break, causing the fixture to fall.

    Product
    Light chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2015·2015-02-04

    Innokas Medical VC150 Vital Signs Monitor Recalled for Alarm Failure

    Innokas Medical is recalling 20 VC150 Vital Signs Monitors because they may fail to issue visual and audible alarms when SpO2 or RRa values violate limits during mode switching.

    Product
    VC150 Vital Signs Monitor (VC150 monitor equipped with Masimo SpO2 technique only); Innokas Medical CARESCAPE VC150 Rx Only Innokas Medical Oy. Catalog numbers 2067980-002, 2067980-006, 2067980-010, and 2067980-014.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·15V065000·2015-02-04

    Morgan Olson Recalls 2014 Service Body Trucks for Lighting Defects

    Morgan Olson is recalling 11 model year 2014 Service Body trucks because rear identification and license plate lamps may be mounted incorrectly, reducing visibility.

    Product
    MORGAN OLSON — MORGAN OLSON SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V066000·2015-02-04

    Piaggio Recalls Vespa and Piaggio Motorcycles Due to Fuel Pump Defect

    Piaggio is recalling specific Vespa and Piaggio motorcycles because a defective fuel pump may cause the vehicle to stall or fail to restart, increasing crash risk.

    Product
    VESPA — VESPA, PIAGGIO LX 150, GTS SUPER 250, GTV 250, BV 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1011-2015·2015-02-04

    Philips BrightView MRI Systems Recalled for Unintended Movement

    Philips is recalling 1,064 BrightView MRI systems worldwide due to software issues causing unintended detector and gantry movement.

    Product
    BrightView model number: 882478 BrightView X model number: 882480 BrightView XCT model number: 882482 and 882454 Medical Device for imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1014-2015·2015-02-04

    Clinical Innovations Recalls Ebb Complete Tamponade System Due to Balloon Leak Risk

    Clinical Innovations, LLC is recalling 827 units of the Ebb Complete Tamponade System because of a potential for balloon leaks in lots manufactured since August 2014.

    Product
    Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1016-2015·2015-02-04

    Mobius Airo Mobile Intraoperative CT System Recalled for Data Transfer Errors

    Mobius Imaging is recalling 21 Airo Mobile Intraoperative CT systems because a software error may cause incorrect or missing navigation data to transfer to the Brainlab Curve system.

    Product
    Airo Mobile Intraoperative CT I Airo; Model #: MobiCT-32. Computed Tomography x-ray system.
    Category
    Medical Device
    Distribution
    10 states