The Recall Desk

Hazard

Abrasion recalls

19 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
19
Critical
0
Severe
0
Most recent
2025-05-21

Of the 19 abrasion recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all abrasion recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–19 of 19

  • HighFDA (Devices)·Z-1780-2025·2025-05-21

    Philips Intera 3.0T Quasar Dual MRI Scanner Coil Seal Adhesive Failure

    Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.

    Product
    Intera 3.0T Quasar Dual, Model Number: 781150;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1773-2025·2025-05-21

    Philips Intera 1.0T MRI Quadrature Body Coil Seal Failure Recall

    Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.

    Product
    Intera 1.0T Power/Pulsar, Model Number: 781103;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1783-2025·2025-05-21

    Philips SmartPath to dStream 3.0T MRI Coil Adhesive Failure Recall

    Philips is recalling SmartPath to dStream 3.0T MRI systems (Model 782145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.

    Product
    SmartPath to dStream for 3.0T, Model Number: 782145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1770-2025·2025-05-21

    Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal

    Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.

    Product
    Enterprise 1.5T, Model Number: 781145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2025·2025-01-22

    Esteem Synergy Stomahesive Skin Barrier pre-cut wafers wrong size

    ConvaTec's Esteem Synergy Stomahesive Skin Barrier packages may contain pre-cut wafers of 28mm instead of the labeled 16mm or 35mm, potentially causing skin abrasion or bleeding during use.

    Product
    Esteem Synergy Stomahesive Skin Barrier, part of Esteem synergy, which is a two-piece ostomy system consisting of an adhesive skin barrier and an adhesive pouch: ESTEEM SYN FLX WHT16/35MM PRECUT(1X10), REF: 405473; ESTEEM SYN FLX WHT35/35MM PRECUT(1X10), REF: 405479
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0952-2024·2024-02-07

    Philips MRI Scanner Quadrature Coil Seal Adhesive May Fail and Create Sharp Edges

    Philips Intera 1.5T Achieva Nova MRI machines (Model 781172) may develop seal adhesive failure in the Quadrature Body Coil, creating sharp edges that could injure patients during scanning.

    Product
    Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0945-2024·2024-02-07

    Philips Achieva MRI Scanner Recall: Loose Coil Seals May Cause Skin Injury

    Philips is recalling Achieva 1.5T MRI scanners due to a seal adhesive defect on the body coil that may fail during scanning, creating sharp edges that risk skin injury including abrasions and lacerations.

    Product
    Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0954-2024·2024-02-07

    MRI Machine Coil Seal Adhesive May Create Sharp Edges

    The Intera Achieva 1.5T Pulsar MRI machine's Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients. All units of this model are affected.

    Product
    Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22003·2021-10-06

    ElliptiGO Arc Bicycles Recalled for Structural Frame Failure Risk

    ElliptiGO Arc bicycles are being recalled because the aluminum frame can break while riding, creating a fall hazard. Six minor injuries have been reported so far.

    Product
    ElliptiGO Arc bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2800-2020·2020-08-19

    United Imaging Recalls uMI 550 PET/CT Systems Due to Imaging and Safety Defects

    Shanghai United Imaging Healthcare is recalling four uMI 550 PET/CT systems due to defects that may cause image artifacts, scanning interruptions, or sharp edges.

    Product
    uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and di
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20005·2019-10-04

    SPRI Ultra Heavy Resistance Bands Recalled for Injury Hazard

    Fit for Life is recalling SPRI Ultra Heavy Resistance Bands because they can separate from handles and strike users, causing injuries.

    Product
    SPRI Ultra Heavy Resistance Bands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1814-2017·2017-04-19

    Aesculap Minop InVent 30 Trocar System Recalled for Sharp Edges

    Aesculap Implant Systems LLC is recalling the Minop InVent 30 Trocar System because sharp edges may abrade insulation during use.

    Product
    AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateCPSC·07069·2006-12-27

    Regal Lager Recalls Phil & Teds e3 Strollers Due to Abrasion Hazard

    Regal Lager is recalling about 14,300 Phil & Teds e3 strollers with doubles seats because children in the lower add-on seat can touch the rear tires, posing an abrasion hazard.

    Product
    Phil & Teds e3 Strollers with doubles seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·02542·2002-05-30

    Sportsman's Guide Recalls Big Red Wagons Due to Wheel Explosion Risk

    The Sportsman's Guide is recalling Big Red Wagons because the plastic wheel rims may break and explode under pressure, posing a risk of injury to nearby individuals.

    Product
    Big Red Wagons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·02160·2002-05-16

    Fitness Quest Recalls Total Gym Exercise Machines Due to Handle Detachment

    Fitness Quest Inc. is recalling Total Gym 1000 and Pro exercise machines because handles can detach and cables can break, causing injuries.

    Product
    Total Gym® 1000 and the Total Gym® Pro model exercise machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide