The Recall Desk

Hazard

Fall Injury recalls

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

What the numbers show

Total
646
Critical
9
Severe
145
Most recent
2026-10-21

Of the 646 fall injury recalls we have scored against our rubric, 9 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 145 (22%) 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 fall 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 646

  • HighNHTSA·22V076000·2022-02-10

    2022 Thor Motor Coach Motorhomes Rear Ladder Installation Defect Recall

    Thor Motor Coach is recalling 2022 ACE, Freedom Traveler, Hurricane, and Windsport motorhomes. The rear ladder may have been installed on the wrong side, which could break while in use and cause injury.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, FREEDOM TRAVELER, HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V016000·2022-01-18

    2022 Peterbilt 579 chassis step bolts may loosen and cause injury

    Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22030·2021-12-15

    Schwinn Tone Electric Scooters recalled for fall and injury hazards

    Pacific Cycle is recalling about 11,340 Schwinn Tone electric scooters because the handlebar grips can loosen or crack, causing falls and injuries. One consumer fell and sustained bruising and abrasions when the handlebar broke during use.

    Product
    Schwinn Tone Electric Scooters (e-scooters)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2600-2021·2021-10-06

    Patient Lift Device Stretch Leveller May Lose Horizontal Position Control

    Hill-Rom LikoStretch 1900 patient lift devices may lose their ability to maintain horizontal position during lifting, risking patient falls. Affected devices can cause patients to slide out of the lift sheet.

    Product
    LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·22004·2021-10-06

    Hobby Lobby White Wood Stools Recalled for Fall and Injury Hazards

    Hobby Lobby is recalling about 14,000 White Wood Stools sold nationwide from June through July 2021 because the stools can break during use, posing fall and injury hazards. Hobby Lobby has received seven reports of the stool breaking, including six resulting in minor injuries.

    Product
    White Wood Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V738000·2021-09-23

    Ducati Recalls 2019 Hypermotard 950 SP for Side Stand Welding Defect

    Ducati is recalling 2019 Hypermotard 950 SP motorcycles because the side stand may be improperly welded. A broken stand could cause the motorcycle to fall, increasing injury risk.

    Product
    DUCATI — DUCATI HYPERMOTARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21184·2021-08-18

    TJX Recalls Swivel Counter Stools Due to Fall and Injury Hazards

    TJX Companies is recalling about 4,300 swivel counter stools sold at HomeGoods and Homesense stores because they can break or collapse, causing falls. The company has received 20 reports of stools breaking, including 17 reports of minor injuries.

    Product
    Swivel Counter Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2208-2021·2021-08-18

    Stryker Prime Big Wheel Stretcher distributed to home users may lack professional-only guidance

    The Prime Big Wheel Stretcher was distributed to home users, but is intended for professional healthcare facility use only. Home users may not understand the professional-only instructions, creating safety risks.

    Product
    Prime Big Wheel Stretcher-used as a short-term outpatient clinical evaluation, treatment, minor procedure, and short-term outpatient recovery platform, Model Number 1115, Part Number 1115000030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2157-2021·2021-08-04

    Zippie Voyage Early Intervention Stroller Seating System May Detach

    Sunrise Medical recalls Zippie Voyage early intervention strollers because the seating system may unexpectedly detach and fall, causing injury. Approximately 9,865 devices are affected.

    Product
    Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V371000·2021-05-20

    2021 Forest River Columbus Dining Chair Legs May Detach During Use

    The Allure Swivel Dining chair legs in 2021 Forest River Columbus trailers may detach, creating an injury risk if occupied. Dealers will install reinforcing hardware free of charge.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21747·2021-05-13

    Leisure Time Recalls Brutus Swing Sets Due to Injury Hazard

    Leisure Time Products is recalling about 9,000 Brutus metal swing sets because the swing hanger attachment can fail, causing the swing to fall.

    Product
    Backyard Discovery Big Brutus, Little Brutus and Mini Brutus metal A-frame swing sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because table fastening bolts may loosen, causing the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1272-2021·2021-03-24

    Accuray CyberKnife Treatment Delivery System Recalled for Loose Set Screws

    Accuray is recalling 243 CyberKnife Treatment Delivery Systems because set screws can loosen, allowing the treatment couch to roll unexpectedly.

    Product
    CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2021·2021-03-24

    Canon Medical Recalls Catheterization Tables Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because loose bolts may cause the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 interventional angiography systems because the table may tilt if fastening bolts become loose.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21101·2021-03-24

    Beal Birdie Belay Devices Recalled Due to Risk of Climber Injury

    Beal Sas is recalling about 1,400 Birdie Belay Devices because the hand lever can detach, preventing users from lowering climbers. No injuries have been reported.

    Product
    Beal Birdie Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0925-2021·2021-02-10

    Hill-Rom Liko Multirall 200 Overhead Lifts Recalled for Detachment Risk

    Hill-Rom is recalling Liko Multirall 200 overhead lifts because a strap lock may not fully engage, causing the lift to detach from the rail and potentially drop the patient.

    Product
    Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0096-2021·2020-10-21

    Handicare SwiftHook Component Recall for Mobile and Ceiling Lifts

    Handicare AB is recalling SwiftHook components used in mobile and ceiling lifts because the carry bar may detach during use, posing a risk of injury to patients and caregivers.

    Product
    SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V500000·2020-08-24

    ETI Recalls 2020 Aerial Lift Trucks Due to Boom Tube Weld Defects

    Equipment Technology is recalling 2020 ETI ETC 37 IH aerial lift trucks because improper welds and steel thickness may cause the platform to fall unexpectedly.

    Product
    ETI — ETI ETC 37 IH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20150·2020-07-16

    Rocky Mountain Recalls Alloy Instinct and Pipeline Bicycles Due to Frame Cracking

    Rocky Mountain is recalling about 1,530 non-electric alloy frame Instinct and Pipeline bicycles because the front frame triangle can crack, posing fall and injury hazards.

    Product
    Rocky Mountain non-electric alloy frame Instinct, Instinct BC and Pipeline bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2326-2020·2020-06-17

    Canon Medical System Recalls 24 Infinix-8000C Digital Radiography Systems

    Canon Medical System is recalling 24 Infinix-8000C digital radiography systems because loose bolts may cause the catheterization table to tilt.

    Product
    Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2325-2020·2020-06-17

    Canon Medical System Recalls Infinix-8000V Catheterization Tables Due to Loose Bolts

    Canon Medical System is recalling 46 Infinix-8000V systems because loose bolts may cause the catheterization table to tilt.

    Product
    Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2327-2020·2020-06-17

    Canon Medical System Recalls Infinix-8000F Fluoroscopy Systems Due to Loose Bolts

    Canon Medical System is recalling 15 Infinix-8000F digital radiography systems because loose bolts may cause the catheterization table to tilt.

    Product
    Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
    Category
    Medical Device
    Distribution
    Distributed nationwide