The Recall Desk

Hazard

Impact Injury recalls

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

What the numbers show

Total
369
Critical
9
Severe
64
Most recent
2026-09-30

Of the 369 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.

201–225 of 369

  • SevereFDA (Devices)·Z-0210-2015·2014-11-19

    Fisher and Paykel Infant Warmer Recall Due to Heater Head Breakage

    Fisher and Paykel Healthcare is recalling IW900-Series Infant Warmers and spare parts because a broken nut may allow the heater head to swing and injure infants.

    Product
    Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and Paykel; Healthcare CosyCot and Kit Replacement Head Case Assembly It is designed to assist with the thermoregulation of infants weighing up to 10kg and is used by labor and delivery rooms and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14E079000·2014-11-19

    AFX Recalls FX-76 Motorcycle Helmets for Impact Test Failure

    AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2015·2014-11-19

    GE Healthcare Recalls Brivo NM615 Nuclear Imaging Systems Due to Loose Fasteners

    GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system. Models H3100TP, H3100TN, H3100TT, H3100TR, H3100TW, H3100WZ, H2401MP, H2401MN, H2401MT, H2401MR, H2401MW, H2401NJ. Product Usage: The Brivo NM 615 is an emission computed tomography system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14270·2014-09-04

    JVC 42-Inch Flat Panel Televisions Recalled for Tip-Over Risk

    AmTRAN Video is recalling JVC 42-inch flat panel televisions because the stand neck can crack, causing the TV to tip over and pose an impact injury risk.

    Product
    JVC 42-inch flat panel televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14251·2014-08-06

    Vizio Recalls 39- and 42-Inch E-Series Televisions Due to Tip-Over Risk

    Vizio is recalling about 245,000 39- and 42-inch E-Series televisions because the stand assembly can fail, causing the TV to tip over and pose an impact injury risk.

    Product
    VIZIO E-Series 39-inch and 42-inch televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1810-2014·2014-06-25

    Walmart Recalls Fifteen Pairs of Safety Glasses for Thickness Defects

    Walmart is recalling 15 pairs of safety glasses that failed to meet required industrial lens thickness and lacked OSHA markings.

    Product
    Safety glasses made with "Rage" frames manufactured between February 20, 2014 and February 25, 2014. The color of the frames of the recalled glasses were either white or black. Safety Eye wear
    Category
    Consumer Product
    Distribution
    12 states
  • HighCPSC·14141·2014-03-26

    SATCO Recalls KolourOne LED Light Bulbs Due to Injury Risk

    SATCO Products is recalling KolourOne LED light bulbs because the metal housing can separate and fall, posing a risk of injury to bystanders.

    Product
    KolourOne Brand Panel Array 2.0 and DUO 2.0 PAR LED Light Bulbs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14081·2014-01-16

    Philips Selecon Recalls Stage Light Barndoors Due to Impact Hazard

    Philips Selecon is recalling four- and eight-leaf barndoors for Rama stage lights because heat can cause them to detach and fall, posing an impact injury risk.

    Product
    Stage Light Barndoors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14066·2013-12-19

    Red Wing Recalls Steel Toe Work Boots Due to Impact Hazard

    Red Wing Shoe Company is recalling approximately 114,000 pairs of steel toe work boots because the toe caps may fail to protect feet during impact.

    Product
    Steel toe work boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0335-2014·2013-11-27

    Philips Brilliance iCT CT Scanner Recall for Footrest Contact Hazard

    Philips is recalling nine Brilliance iCT CT scanners because the footrest extension can contact the gantry or user during operation.

    Product
    Brilliance iCT Computed Tomography X-Ray System, Product Usage: The Brilliance iCT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2271-2013·2013-10-02

    Stryker Vision Mounting Arm Recalled Due to Display Detachment Risk

    Stryker Endoscopy is recalling 14,271 Vision Mounting Arms because excessive force can cause the display to detach and fall on users or patients.

    Product
    Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model number 0240-095-200, manufactured by Stryker Endoscopy San Jose The intended use of the Stryker Vision Mount is to hold and position an LCD monitor. The…
    Category
    Medical Device
    Distribution
    51 states
  • HighNHTSA·13E047000·2013-08-16

    Tegol Motorcycle Helmets Recalled for Failing Federal Safety Standards

    Tegol is recalling AX-3, AX-4, and TG-5 Series Outlaw motorcycle helmets because they fail to meet federal safety requirements for impact and retention.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1848-2013·2013-08-07

    Siemens Luminos dRF Fluoroscopic X-Ray System Recalled for Software Error

    Siemens is recalling four Luminos dRF Fluoroscopic X-Ray systems due to a software error that may cause the table to tilt and collide with the floor.

    Product
    Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·13746·2013-08-07

    LSI Recalls Wind Speed Sensors Due to Risk of Injury from Impact

    Load Systems International is recalling LSI model GS025 wind speed sensors because they may fail to display accurate data, posing a risk of injury from impact.

    Product
    LSI Wind Speed Sensors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·13244·2013-07-23

    Kids II Recalls Baby Einstein Activity Jumpers Due to Impact Hazard

    Kids II is recalling Baby Einstein Musical Motion Activity Jumpers because the sun toy attachment can snap backward and injure infants.

    Product
    Baby Einstein Musical Motion Activity Jumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·13225·2013-06-25

    Bel Air Lighting Recalls Chandeliers Due to Falling Hazard

    Bel Air Lighting is recalling about 20,500 nine-light chandeliers because the mounting loop can break, causing the fixture to fall and pose an impact injury hazard.

    Product
    Portfolio and Transglobe nine-light chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13226·2013-06-25

    Genlyte Recalls Capri Track Lighting Due to Impact Injury Hazard

    Genlyte is recalling about 80,300 Capri track lighting fixtures because they can fall off the track rail, posing an impact injury hazard to bystanders.

    Product
    Capri track lighting
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13222·2013-06-20

    Kichler Aztec Chandeliers Recalled for Falling Hazard

    Kichler Lighting is recalling Aztec chandeliers sold at Lowe's because the fixture loop can fail, causing the light to fall from the ceiling.

    Product
    Aztec Light Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide