The Recall Desk

Hazard

Injury recalls

1,366 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,366
Critical
6
Severe
415
Most recent
2026-09-03

Of the 1,366 injury recalls we have scored against our rubric, 6 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 415 (30%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injury 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.

1076–1100 of 1366

  • HighNHTSA·12V564000·2012-12-06

    Prevost Recalls 2011-2012 X3-45 Coach Buses Due to Fire Suppression Defect

    Prevost is recalling 87 model year 2011-2012 X3-45 coach buses because high engine temperatures may cause the fire suppression system to release prematurely, potentially preventing it from operating during a fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13059·2012-12-06

    Ridgid Pneumatic Nailers Recalled Due to Laceration Hazard

    One World Technologies is recalling Ridgid pneumatic nailers sold at Home Depot because the trigger assembly can malfunction and discharge fasteners, posing an injury risk.

    Product
    RIDGID Coil Roofing Nailer and RIDGID Clipped Head Framing Nailer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0440-2013·2012-12-05

    Cooper Surgical Recalls Advincula Arch Uterine Manipulator Handles

    Cooper Surgical is recalling Advincula Arch handles because the internal steel rod may protrude through the shaft, posing a risk of injury during surgery.

    Product
    Cooper Surgical Advincula Arch , Reusable Uterine Manipulator Handle Ref: UMH750 The intended use of the RUMI Arch is in an operative endoscopy (laparoscopy) where a uterus is present and where positioning of the uterus, fallopian tubes and ovaries is desirable. These types
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0380-2013·2012-11-28

    Stryker XIA 3 Torque Wrench Recalled Due to Hex Tip Fracture

    Stryker Spine is recalling 54 XIA 3 Torque Wrenches because the hex tip may fracture during use, posing a risk of injury to patients or providers.

    Product
    Stryker XIA 3 TORQUE WRENCH REF 48237028 Manufactured by: Stryker pine SAS Z.I MARTICOT-33610-CESTAS-FRANCE +33 (0)5.57.97.06.30 http://www.stryker.com Distributed in the USA by: Stryker Spine, 2 Pearl Ct. Allendale NJ 07401-1677 USA +1-201-780-8000 The Xia 3/
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13052·2012-11-28

    Sportspower Recalls Children's Waterslides Due to Injury Hazard

    Sportspower is recalling Liquid Motion waterslides sold at Menards because inadequate warning labels pose a risk of serious neck injuries.

    Product
    Liquid Motion waterslides
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0428-2013·2012-11-28

    IMRIS OR Tables Recalled Due to Magnet Attraction Risk

    IMRIS is recalling ORT100 and ORT200 tables used in MRI systems because the foot end may be attracted to the magnet, posing a risk of injury to patients and operators.

    Product
    IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and Neuro III-SV Magnetic Resonance Imaging Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13050·2012-11-28

    G-U Hardware Recalls Window Fittings Due to Injury Hazard

    G-U Hardware is recalling approximately 5,000 window fittings because they can break, causing windows to fall and posing an injury hazard.

    Product
    Window Fittings: Tilt-turn Stay Arms and Side-hung Sash Hinges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V504000·2012-10-17

    BMW Recalls 7-Series Vehicles for Door Latch Software Defect

    BMW is recalling 2005-2007 7-Series vehicles because a software issue may cause doors to open unexpectedly while driving, posing a risk of occupant ejection or injury.

    Product
    BMW — BMW 760I, 750I, 745I, 750LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2484-2012·2012-10-10

    Zimmer Recalls Provisional Femoral Heads Due to Fit Issues

    Zimmer, Inc. is recalling provisional femoral heads used in hip surgery due to reports of sub-optimal fit with mating components.

    Product
    00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780304003 MIS 12/14 Slotted Femoral Head Provisional +3.5X36 00780304004 MIS 12/14 Slotted Femoral Head Provisional +7X36 00780304005 MIS 12/14 Slotte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V485000·2012-10-04

    Land Rover Recalls 2012 Range Rovers for Windshield Installation Defect

    Land Rover is recalling 2012 Range Rovers because windshields may have been installed incorrectly. This defect could cause the windshield to come loose in a crash, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12E035000·2012-10-02

    Yakima Rooftop Rack Recall for 2012-2013 Ford Focus Vehicles

    Yakima is recalling specific rooftop rack systems for 2012-2013 Ford Focus vehicles because they may slide off when loaded, posing a hazard to others.

    Product
    FORD — FORD FOCUS
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V455000·2012-09-17

    Zero Motorcycles Recalls 2012 S and DS Models for Power Loss Risk

    Zero Motorcycles is recalling 2012 S and DS motorcycles because a motor encoder signal may drift, causing the motor controller to shut off and resulting in a loss of power.

    Product
    ZERO — ZERO ZERO DS, ZERO S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V423000·2012-08-30

    Altec Recalls 2011-2012 Digger Derrick Vehicles Due to Shaft Defect

    Altec Industries is recalling 2011-2012 Digger Derrick vehicles with PENGO extensions because a weld defect may cause the shaft to separate, risking injury or property damage.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12E030000·2012-08-20

    BESI Recalls Pro-Tech III Child Securement Systems for School Buses

    BESI is recalling Pro-Tech III child securement systems for school buses because one buckle can be pulled out with minimal pressure, potentially failing to restrain occupants in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12249·2012-08-16

    Emerson Corsair Ceiling Fans Recalled Due to Falling Hazard

    Emerson is recalling Corsair ceiling fans because the hanger bracket can spread apart, causing the fan to fall from the ceiling.

    Product
    Emerson Corsair Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12744·2012-08-16

    PBteen Recalls Beadboard Bunk Beds Due to Risk of Injury

    PBteen is recalling Beadboard Bunk Beds because the front upper horizontal panel can crack or break, posing a risk of injury.

    Product
    Beadboard Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2155-2012·2012-08-15

    Stryker Luxor Retractor Base Recalled Due to Blade Disassembly

    Stryker Spine is recalling 30 Luxor Retractor Base devices because blades may disassemble from the base, causing the retractor to collapse during use.

    Product
    LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the USA by: Stryker Spine. 2 Pearl Ct. Allendale, NJ 07401. Provides access to the thoracic and lumbar spine from a posterior approach via a sma
    Category
    Medical Device
    Distribution
    0 states