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.

901–925 of 1366

  • HighNHTSA·15V510000·2015-08-12

    Winnebago Recalls 2014-2015 Motorhomes Due to Stuck Deadbolt Locks

    Winnebago is recalling 2014-2015 Itasca and Winnebago motorhomes because deadbolt locks may become stuck, potentially trapping occupants inside the vehicle.

    Product
    ITASCA — ITASCA, WINNEBAGO SPIRIT, VISTA, BRAVE, MINNIE WINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V500000·2015-08-10

    GM Recalls 2010 Chevrolet Cobalt Vehicles for Air Bag Wiring Defect

    General Motors is recalling 2010 Chevrolet Cobalt vehicles because a misrouted wiring harness may disable the driver-side curtain air bag, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET COBALT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2015·2015-08-05

    Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling

    The Anspach Effort, Inc. is recalling 99 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual usage, potentially resulting in greater exposure than specified.

    Product
    ANSPACH -4MM Coarse Diamond Ball, 22MM Shaft Exposure; REF S-4DC-22-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-2289-2015·2015-08-05

    Anspach Diamond Ball Tools Recalled for Inconsistent Shaft Exposure Labeling

    The Anspach Effort, Inc. is recalling 72 Anspach Extra Coarse Diamond Ball tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.

    Product
    ANSPACH - Extra Coarse Diamond Ball; 8MM REF L-8DX-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-2283-2015·2015-08-05

    Anspach Fluted Drum Dissection Tools Recalled for Inconsistent Shaft Exposure

    The Anspach Effort, Inc. is recalling 177 fluted drum dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.

    Product
    ANSPACH - Fluted Drum, Side Cut only, 6MM x 14MM REF L-6DRC-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • SevereNHTSA·15V485000·2015-08-04

    New Flyer Recalls NABI Transit Buses Due to Pressure Relief Defect

    New Flyer is recalling specific 2014-2015 NABI transit buses because pressure relief devices may fail to vent gas, increasing the risk of tank explosion, fire, and injury.

    Product
    NABI — NABI 40LFW, 42BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2120-2015·2015-07-29

    GE Healthcare Precision 500D Monitor Suspension Recall

    GE Healthcare is recalling Precision 500D and related fluoroscopic systems because monitor suspensions may fail, posing a risk of injury to patients or operators.

    Product
    GE Healthcare Precision 500D Classical R & F system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E058000·2015-07-14

    Agility Fuel Systems Recalls CNG Fuel Systems Due to Pressure Relief Defect

    Agility Fuel Systems is recalling certain compressed natural gas (CNG) fuel systems because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E059000·2015-07-14

    Emcara Pressure Relief Devices Recalled for CNG Tank Explosion Risk

    Emcara is recalling specific Pressure Relief Devices (PRDs) that may fail to vent pressure, potentially causing CNG tank explosions, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1966-2015·2015-07-08

    GE Healthcare Radiographic Systems Recalled for Safety Mechanism Failure

    GE Healthcare is recalling Precision 500D and Advantx Legacy systems because a safety mechanism may fail to engage, posing a risk of injury from falling equipment.

    Product
    GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic imaging system for radiographic and fluoroscopic examinations. Applications can be performed with the patient sitting, standing, or lying in the prone or sup
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1847-2015·2015-07-08

    Medtronic Recalls Navigated Cannulated Taps Due to Cleaning Injury Risk

    Medtronic Navigation is correcting 15,798 Navigated Cannulated Taps distributed worldwide due to a potential for injury during the cleaning process.

    Product
    Medtronic Navigated Cannulated Taps Individual cannulated taps are packaged in a clear plastic tube with protective plastic end caps. Kit/sets contain various devices including the taps. The kit/set configuration varies dependent on the part number. The devices are assembled a
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1848-2015·2015-07-08

    Pega Medical Recalls SCFE Drivers Due to Handle Detachment Risk

    Pega Medical Inc. is recalling four units of SCFE Drivers because the handle may detach from the shaft during use.

    Product
    Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Screw System with catalogue number SCF-MLD265 and SCF-MLD273.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1820-2015·2015-07-01

    Hill-Rom Steriseal-Cannula Ophthalmic Recall Due to Dislodgement Risk

    Hill-Rom is recalling Steriseal-Cannula Ophthalmic handpieces because the metal cannula can rotate and become dislodged from the plastic handpiece.

    Product
    Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·15737·2015-06-30

    Yamaha Recalls SRViper Snowmobiles Due to Brake Failure Risk

    Yamaha is recalling about 200 SRViper snowmobiles because the brake line can contact the clutch, causing brake failure and posing a risk of injury or death.

    Product
    Yamaha SRViper snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15173·2015-06-30

    Technosport Recalls Omersub Scuba Mask Due to Shattering Lens Hazard

    Technosport is recalling Omersub Zero Cube scuba masks because non-conforming glass lenses can shatter during normal use, posing an injury hazard.

    Product
    Omersub Zero Cube scuba diving mask
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1727-2015·2015-06-17

    CooperSurgical Ally Uterine Positioning System Recalled for Injury Risk

    CooperSurgical is recalling five Ally Uterine Positioning System units because the design may expose users to injury to fingers or body parts.

    Product
    Ally Uterine Positioning System (Ally UPS) used in the mounting and positioning and holding of uterine manipulators during gynecological laproscopic procedures Model: Ally UPS
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·15152·2015-05-28

    GT Fury Mountain Bicycles Recalled Due to Front Wheel Hub Failure Risk

    Cycling Sports Group is recalling 2015 GT Fury Elite and Expert downhill mountain bicycles because the front wheel hub can break, causing disc brake failure and crash hazards.

    Product
    GT downhill mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1553-2015·2015-05-06

    Synthes Small Battery Drive Oscillating Saw Attachment Recall

    The Anspach Effort, Inc. is recalling Synthes Small Battery Drive Oscillating Saw Attachments because they may disengage during surgery, posing a risk of injury.

    Product
    Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide