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.

76–100 of 368

  • ModerateCPSC·22033·2021-12-15

    Ceiling Fans Recalled Due to Detaching Blades Impact Injury Risk

    About 77,900 Harbor Breeze Belleisle Bay and Honeywell Rio ceiling fans are recalled because the blades can detach during use and strike consumers or cause property damage.

    Product
    Harbor Breeze Belleisle Bay and Honeywell Rio Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0279-2022·2021-12-01

    PET/CT Imaging System Ceiling Mount May Detach Due to Bracket Wear

    Philips TruFlight Select PET/CT imaging systems have a Monitor Bracket Assembly that may detach from the ceiling mount due to undetected shaft wear, posing a risk of injury to patients, staff, and bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - TruFlight Select PET/CT System Number: 882438 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0280-2022·2021-12-01

    Philips CT Fluoroscopy Ceiling Mount Bracket Wear and Detachment Hazard

    Philips Continuous CT Fluoroscopy ceiling mounts may experience monitor bracket assembly wear that goes undetected, potentially causing the bracket to detach and fall on patients, operators, or bystanders during surgery.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 16 System Number: 882470 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·22022·2021-11-23

    Impex Fitness Olympic Dumbbell Handles Recalled for Impact Injury Hazard

    Impex Fitness is recalling about 77,200 Olympic Dumbbell Handles because the locking collars can slip, causing weights to drop and potentially cause impact injuries. No injuries have been reported to date.

    Product
    Olympic Dumbbell Handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2021·2021-07-07

    Monitor Bracket Assembly Wear May Cause Fall Hazard for Medical Imaging Equipment

    Philips medical imaging equipment monitor bracket assemblies may detach due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2021·2021-07-07

    Philips CT Monitor Bracket Assemblies Recalled for Detachment Risk

    Philips has recalled 1,301 Monitor Bracket Assemblies for CT systems worldwide due to shaft wear that could cause monitors to detach and fall, potentially injuring patients, operators, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728333 - Spectral CT:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1980-2021·2021-07-07

    Philips Continuous CT Fluoroscopy Monitor Bracket Assembly Fall Risk

    Philips is recalling 1,301 Monitor Bracket Assemblies due to shaft wear that could cause the assembly to detach from the ceiling suspension arm. This could result in the monitor falling and causing serious injury to patients, operators, bystanders, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and MX16 Models: 728131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1984-2021·2021-07-07

    Philips CT Monitor Bracket Assembly May Detach and Fall

    Philips is recalling 1,301 monitor bracket assemblies for CT imaging systems due to shaft wear that could cause detachment and fall of the monitor. This could result in serious injury to patients, operators, and staff.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Ingenuity Core, Ingenuity Core 128, Ingenuity CT 728321 - Ingenuity Core 728323 - Ingenuity Core 128 728326/728327 - Ingenuity CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2021·2021-07-07

    Philips Medical Monitor Bracket May Detach from Ceiling Mount

    Philips medical imaging monitors with worn bracket assembly shafts may detach from ceiling suspensions and fall on patients, operators, or staff. No injuries have been reported.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882476 - Gemini TF Big Bore PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V325000·2021-05-07

    Airstream Globetrotter Travel Trailers Cabinet Door Adhesive Failure Recall

    Airstream is recalling 2020-2021 Globetrotter travel trailers because adhesive on overhead cabinet doors may fail, causing the doors to fall and potentially injure occupants.

    Product
    AIRSTREAM — AIRSTREAM GLOBETROTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21075·2021-02-10

    Bowflex SelectTech Barbells Recalled Due to Impact Injury Hazard

    Nautilus is recalling Bowflex SelectTech 2080 Barbells with Curl Bar because weight plates can fall off, posing an impact injury hazard.

    Product
    Bowflex SelectTech™ 2080 Barbells with Curl Bar
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2021·2020-12-16

    Shimadzu Mobile X-Ray System Recalled for Improper Handle Bolts

    Shimadzu Medical Systems is recalling 115 Mobile X-Ray Systems because the adjustable handle may have improper bolts, posing a risk of harm to individuals around the device.

    Product
    Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan - Product Usage: The device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergen
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E082000·2020-10-27

    Leather on Wheels Recalls Polo Helmets for Impact Protection Defect

    Leather on Wheels is recalling Polo model helmets because they may not adequately reduce impact force, increasing the risk of injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1564-2020·2020-04-01

    Capintec Captus 4000e Thyroid Uptake System Recall for Collimator Defect

    Capintec is recalling Captus 4000e Thyroid Uptake Systems because insufficiently tapped screw holes may allow the collimator assembly to fall and contact patients or operators.

    Product
    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1445-2020·2020-03-11

    Stryker Connected OR Cart Recalled Due to Monitor Attachment Defect

    Stryker is recalling 12 Connected OR Carts because the monitor may not attach correctly, posing a risk of the monitor falling and injuring users.

    Product
    Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only, Manufactured for: Stryker, 5900 Optical Court, San Jose, CA 95138, UDI: 07613327462784 - Product Usage: The Connect OR Cart is a mobile, medical-grade cart intended to store and transport components of minimal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0920-2020·2020-02-05

    Mindray BA-800M Chemistry Analyzer Recalled for Gas Spring Failure Risk

    Mindray is recalling seven BA-800M Chemistry Analyzers because a gas spring on the protective cover may fail, posing a low risk of impact injury to users.

    Product
    BA-800M Chemistry Analyzer Part Numbers BA81E-PA00002 and BA81E-PA00003, Containing Gas spring YQ-8/18-90-272-180N (Material Code M6T-010001--- (front spring)) and Gas spring YQ6/15-84-235(B-B)-80N (033-000090-00 (rear spring))
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0921-2020·2020-02-05

    Mindray ABS800 Chemistry Analyzer Gas Spring Recall

    Mindray is recalling six ABS800 Chemistry Analyzers due to a potential gas spring failure that poses a low risk of impact injury to users.

    Product
    ABS800 Chemistry Analyzer Part Number BA81F-PA00001, Containing Gas spring YQ-8/18-90-272-180N (Material Code M6T-010001--- (front spring)) and Gas spring YQ6/15-84-235(B-B)-80N (033-000090-00 (rear spring))
    Category
    Medical Device
    Distribution
    2 states
  • HighCPSC·20024·2019-11-19

    Ontel ISO7X Isometric Exercise Devices Recalled for Projectile Hazard

    United National Closeout Stores is recalling about 1,500 Ontel ISO7X isometric exercise devices because handle grips can break and eject parts, posing an injury risk.

    Product
    ISO7X Isometric Exercise Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19E076000·2019-11-12

    Matrix Alpha Motorcycle Helmets Recalled for Retention System Failure

    Matrix Headgear is recalling Alpha motorcycle helmets because the retention system may fail, allowing the helmet to separate from the head during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide