The Recall Desk

Hazard

Impact Injury recalls

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

What the numbers show

Total
368
Critical
9
Severe
64
Most recent
2026-08-26

Of the 368 impact injury recalls we have scored against our rubric, 9 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 64 (17%) 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 impact 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.

126–150 of 368

  • HighFDA (Devices)·Z-2864-2018·2018-08-29

    Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard

    Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost Upgrades (Stitching Patient Support) 712083
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2852-2018·2018-08-29

    Philips DigitalDiagnost 4.1 Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost 4.1 units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost 4.1 (Stitching Patient Support) 712225
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2866-2018·2018-08-29

    Philips DigitalDiagnost Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost Single-Detect units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.

    Product
    DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2845-2018·2018-08-29

    Philips DigitalDiagnost Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators or patients.

    Product
    DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2851-2018·2018-08-29

    Philips DigitalDiagnost 4 Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost 4 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.

    Product
    DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2861-2018·2018-08-29

    Philips DigitalDiagnost Release 3 Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.

    Product
    DigitalDiagnost Release 3 (Stitching Patient Support) 712025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2502-2018·2018-07-25

    Maquet VOLISTA StandOP Surgical Light Recall for Detachment Risk

    Maquet is recalling 151 VOLISTA StandOP surgical lights due to a potential light head detachment issue that could cause serious injury.

    Product
    VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF AIM STP; ARD568821911 VLT600SF AIM STP QL; ARD568821910 VLT600SF STP QL; ARD568811901 VLT600SF AIM STP Product Usage: The Maquet VOLISTA surgic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2176-2018·2018-06-20

    Philips Brilliance 16 P CT Systems Recalled for Head Holder Contact Risk

    Philips is recalling 20 Brilliance 16 P CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 16 P with DEPMED HARDENING KIT 12NC: 453567400741, Model Number 728246. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2174-2018·2018-06-20

    Philips Brilliance 64 CT System Recalled for Patient Support Head Holder Hazard

    Philips is recalling three Brilliance 64 CT systems because the patient support head holder could contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2175-2018·2018-06-20

    Philips Brilliance 16 CT System Recalled for Head Holder Contact Hazard

    Philips is recalling two Brilliance 16 CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 16 with DEPMED HARDENING KIT 12NC: 453567400741, Model Number 728240. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1318-2018·2018-04-18

    Reliance Medical Products Recalls Refractor Suspension Arms Due to Missing Parts

    Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.

    Product
    Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a refractor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18129·2018-03-22

    SpeeCo and Woods Recall 4-Way Wedge Accessory for Log Splitters

    SpeeCo and Woods are recalling 4-way wedge accessories for hydraulic log splitters because they can detach and strike users, causing injury.

    Product
    4-way wedge accessory for hydraulic log splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0595-2018·2018-02-21

    Hologic Panther Fusion Recalled Due to Falling Glass Panel Hazard

    Hologic is recalling 103 Panther Fusion instruments because the glass panel may separate from the monitor and fall, potentially striking an operator.

    Product
    Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 Product Usage: The Panther instrument is a fully automated sample-to-result instrument, eliminating the need for batch processing and automates all aspects of nucleic acid testing on a single, integrated platform. The Pa
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0311-2018·2018-01-10

    Philips Mobile Detector Holder Recalled Due to Potential Detector Drop Hazard

    Philips is recalling 412 Mobile Detector Holders for Stationary X-ray Systems because the lock mechanism may fail, causing the detector to drop.

    Product
    Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable detector free in the room for X-ray exposures. It supports the wireless portable detector with or without a grid.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·18713·2018-01-04

    SureFit Recalls Riding Lawn Mower Blade Spindle Shafts Due to Impact Hazard

    SureFit is recalling about 900 riding lawn mower blade spindle shafts and assemblies because they can break and become projectiles, posing an impact injury risk.

    Product
    SureFit™ riding lawn mower blade spindle shafts and assemblies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18062·2017-12-14

    Hunter Contempo Ceiling Fans Recalled for Impact Injury Hazard

    Hunter Fan Company is recalling Contempo ceiling fans because incorrect installation instructions may cause the light globe to fall, posing an impact injury hazard.

    Product
    Hunter Contempo ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18050·2017-11-30

    Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard

    Flos Inc. is recalling specific Romeo Moon and Romeo Louis II pendant light fixtures because the internal glass diffuser can detach and fall, posing an impact injury hazard.

    Product
    Pendant light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V624000·2017-10-04

    Transtech Recalls 2015-2016 School Buses Due to Seat Padding Defect

    Transportation Collaborative is recalling 2015-2016 Trans Tech school buses because seat mounting studs lack adequate padding, increasing injury risk in rear-end collisions.

    Product
    TRANS TECH BUS — TRANS TECH BUS ST AERO, SST FLR, STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V558000·2017-09-08

    Micro Bird Recalls 2016 G5 School Buses for Seat Safety Defect

    Micro Bird is recalling 25 units of 2016 G5 school buses because seat mounting studs may lack adequate padding, increasing injury risk in rear-end collisions.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17118·2017-03-31

    Black+Decker Portable Table Saws Recalled for Stand Collapse Hazard

    Rexon is recalling Black+Decker portable table saws sold at Walmart because the stand can collapse, posing laceration and impact injury risks.

    Product
    Black+Decker portable table saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17120·2017-03-29

    Juratoys Recalls Janod Push Toy Trolleys Due to Impact Injury Hazard

    Juratoys is recalling four models of Bricolo by Janod push toy trolleys because they can tip backwards, posing an impact injury hazard to children.

    Product
    Bricolo by Janod ® Push toy trolleys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V898000·2016-12-14

    KZRV Recalls 2016-2017 Durango and Venom Trailers for Door Hinge Defect

    KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.

    Product
    KZRV — KZRV DURANGO, VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide