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.

36426–36450 of 50504

  • HighCPSC·16733·2016-03-11

    Room & Board Recalls Doyle Chairs Due to Laceration Hazard

    Room & Board is recalling Doyle arm and side chairs because the backrest can break during normal use, posing a laceration hazard.

    Product
    Doyle arm chairs and side chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V146000·2016-03-10

    Mercedes-Benz Recalls 2016 GLC 300 Vehicles for Wiring Harness Defect

    Mercedes-Benz is recalling 2016 GLC 300 vehicles because a misrouted wiring harness may cause unexpected air bag deployment or engine stalling, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16731·2016-03-10

    Carlin Recalls Williamson and Thermoflo Furnaces and Boilers Due to Fire Hazard

    Carlin is recalling about 110 Williamson and Thermoflo furnaces and boilers equipped with Carlin oil burners because a wiring malfunction can cause the burners to fail to shut off, posing a fire hazard.

    Product
    Williamson-Thermoflo furnaces and boilers equipped with Carlin oil burners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V145000·2016-03-10

    Hyundai Recalls 2016-2017 Santa Fe for Seat Belt Warning Defect

    Hyundai is recalling 34,200 Santa Fe vehicles because damaged wires may prevent the front seat belt warning light from activating, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16732·2016-03-10

    Anchor Industries Recalls Safety Pool Covers Due to Drowning Risk

    Anchor Industries is recalling specific safety pool covers because brass-plated snap hooks can break, posing a drowning risk. No injuries have been reported.

    Product
    Safety pool covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1031-2016·2016-03-09

    Mako Surgical Recalls Restoris Knee Implants Due to Packaging Damage

    Mako Surgical Corporation is recalling 146 units of the Restoris Multicompartmental Knee System because damaged packaging may have compromised the sterile barrier.

    Product
    Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee replacement used in conjunction with RIO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2016·2016-03-09

    Cook Inc. Recalls Kopans Breast Lesion Localization Needles

    Cook Inc. is recalling 134 Kopans Breast Lesion Localization Needles because they may have been exposed to body fluids during processing, posing a potential risk of blood-borne pathogen transmission.

    Product
    Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle with centimeter markings and a hookwire. The hookwire features a burnish mark that allows the operator to ensure that the hookwire is within the needle tip…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2016·2016-03-09

    Philips Recalls BrightView XCT Gamma Cameras Due to Mechanical Defects

    Philips is recalling 427 BrightView XCT gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.

    Product
    BrightView XCT & BrightView XCT Upgrade, gamma cameras; For Single Proton Emission Computed Tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2016·2016-03-09

    Siemens Dimension Vista B2 Microglobulin Reagent Cartridge Recall

    Siemens Healthcare Diagnostics is recalling Dimension Vista B2 Microglobulin reagent cartridges due to increased abnormal assay errors and calibration failures that may produce inaccurate patient results.

    Product
    Dimension Vista System B2 Microglobulin Flex reagent cartridge and urine stabilizer Catalog #K7024 SMN: 10445889 Lot #15246MA Product Usage: The B2MIC method is an in vitro diagnostic test for the quantitative measurement of B2-microglobulin in human serum…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1026-2016·2016-03-09

    Ivoclar Vivadent Recalls Helioseal Clear Pit and Fissure Sealant

    Ivoclar Vivadent is recalling Helioseal Clear dental sealant because a production error may prevent the material from curing properly under specific lights.

    Product
    Helioseal Clear Refill 1 x 1.25 g, REF/Product Code/Art. No. 558521AN and Helioseal Clear Assortment 5 x 1.25 g, REF/Product Code/Art. No. 558520AN ---- COMMON/USUAL NAME: Pit & Fissure Sealant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2016·2016-03-09

    ConvaTec Recalls Opti-Mist Nebulizer Masks Due to Reduced Aerosol Output

    ConvaTec is recalling Opti-Mist and Opti-Mist Clear nebulizer masks because a component defect reduces or stops aerosol output, potentially preventing patients from receiving medication.

    Product
    Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses that are delivered directly to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1045-2016·2016-03-09

    Maquet Extension Device Recalled for Potential Detachment from Operating Table

    Maquet is recalling the 1180.19F0 Extension Device because it may unlock and fall from the MAGNUS operating table.

    Product
    Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, Used to support the upper and lower extremities immediately before, during and after fracture surgery. The Extension Device (1180.19F0) is a table top module for use with the Maquet MAGNUS operating…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1029-2016·2016-03-09

    Argon Medical Devices Recalls ClosureFast Introducer Sheath Sets Due to Assembly Error

    Argon Medical Devices is recalling specific ClosureFast Introducer Sheath Sets because incorrect sheath lengths were assembled to the devices.

    Product
    ClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF MIS-F707 and ClosureFast Introducer Sheath Set 7Fr/Ch(2.3mm) x 11 cm REF IS-7F11. Indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1021-2016·2016-03-09

    Philips Recalls BrightView X Gamma Cameras Due to Motion and Collision Issues

    Philips Medical Systems is recalling 117 BrightView X gamma cameras worldwide due to potential gantry motion halts and collimator contact with the patient pallet.

    Product
    BrightView X are gamma cameras; Designed for single or dual detector nuclear imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16116·2016-03-09

    Z Gallerie Recalls Golda Wall Clocks Due to Fire Hazard

    Z Gallerie is recalling Golda wall clocks because defective battery springs can cause batteries to overheat, posing a fire hazard.

    Product
    Golda Wall Clocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V138000·2016-03-07

    Volkswagen Recalls 2015-2016 e-Golf Vehicles for Battery Software Defect

    Volkswagen is recalling 2015-2016 e-Golf vehicles because oversensitive battery diagnostics may cause the electric motor to shut down unexpectedly, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN E-GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-030716·2016-03-07

    Yummy Chicken Breast Nuggets Recalled for Metal Contamination

    USDA FSIS issued a public health alert for Yummy brand chicken nuggets potentially contaminated with metal pieces. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Imported Chicken Product For Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide