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.

32976–33000 of 50502

  • HighNHTSA·17V159000·2017-03-10

    Kia Recalls 2017 Niro Hybrid for Power Steering Connector Defect

    Kia is recalling 2017 Niro Hybrid vehicles because a damaged steering connector may cause a loss of power steering assist, increasing the risk of a crash.

    Product
    KIA — KIA NIRO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17108·2017-03-10

    R.W. Beckett Recalls Firomatic Fuel Oil Valves Due to Fire Hazard

    R.W. Beckett is recalling approximately 18,000 Firomatic fusible safety valves because the stem may fail to seal, allowing fuel to leak and posing a fire hazard.

    Product
    Firomatic® fusible safety valves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17107·2017-03-09

    Pier 1 Imports Recalls Bistro Chairs Due to Fall Hazard

    Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.

    Product
    Neely and Dahlia Bistro Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V157000·2017-03-09

    Manac Recalls 2016-2017 Van Trailers Due to Failing Rub Rail Rivets

    Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.

    Product
    MANAC — MANAC VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2017·2017-03-08

    Windstone Medical Packaging Recalls Podiatry Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 2,018 Podiatry Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Podiatry Pack, part number AMS2778 Podiatry Pack, part number AMS2778(A Podiatry Pack, part number AMS3785(B Podiatry Pack, part number AMS3785(C Podiatry Pack, part number AMS4011(A Podiatry Pack, part number PSS3422(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1384-2017·2017-03-08

    Beckman Coulter iChemVELOCITY Urine Chemistry System Recalled for Probe Misalignment

    Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.

    Product
    iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2017·2017-03-08

    Windstone Medical Packaging Recalls Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 331 laparotomy packs because the disposable gloves inside may contain splits or holes that compromise sterility.

    Product
    Laparotomy Pack, part number 006268-9 Laparotomy Pack, part number AMS4418(A Laparotomy Pack, part number PSS2190(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1545-2017·2017-03-08

    Bell Stone Toffee Recalls White Chocolate Toffee for Undeclared Milk Allergen

    Bell Stone Toffee is voluntarily recalling White Chocolate Toffee because the label declared butter but failed to identify the presence of the milk allergen.

    Product
    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1322-2017·2017-03-08

    Windstone Medical Knee Scope Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 156 Knee Scope Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1355-2017·2017-03-08

    Windstone Medical Packaging Recalls Ortho Packs with Defective Gloves

    Windstone Medical Packaging is recalling 84 Ortho Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Ortho Pack, part number PSS3466(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1294-2017·2017-03-08

    Windstone Medical ENT Packs Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling 390 ENT Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    ENT Pack, part number AMS3237(A ENT Pack, part number AMS4214
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1388-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Performer Introducer Sets Due to Blood Loss Risk

    Cook Inc. is recalling 854 Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.

    Product
    Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1350-2017·2017-03-08

    Windstone Medical Packaging Recalls Open Procedure Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,125 Open Procedure Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Open Procedure Pack, part number AMS4596 Open Procedure Pack, part number AMS4596(A Open Procedure Pack, part number AMS4596(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1281-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Chest Breast Drape, part number AMS5853
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1380-2017·2017-03-08

    Windstone Medical Recalls Vascular Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling 360 Vascular Packs because the disposable gloves inside may contain splits or holes that compromise sterility.

    Product
    Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1334-2017·2017-03-08

    Windstone Medical Liposuction Kits Recalled for Potential Sterility Compromise

    Windstone Medical Packaging recalled 35 liposuction kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Liposuction Pack, part number AMS3323(B Liposuction Pack, part number AMS5684 Liposuction Pack, part number AMS5699
    Category
    Medical Device
    Distribution
    26 states