The Recall Desk

Hazard

Fall Risk recalls

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

What the numbers show

Total
118
Critical
1
Severe
13
Most recent
2026-08-12

Of the 118 fall risk recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 13 (11%) 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 risk 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.

101–118 of 118

  • HighFDA (Devices)·Z-0416-2015·2014-11-26

    MediChoice Folding Walker Recalled Due to Wheel Defects

    Owens & Minor is recalling MediChoice Dual-Release Folding Walkers because the wheels may be loose, too tight, or fall off.

    Product
    MediChoice Dual-Release Folding Walker with 5" wheel
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0151-2015·2014-11-05

    Joerns EasyCare Bed Recalled Due to Care-Lock Feature Failure Risk

    Joerns Healthcare is recalling 3,135 EasyCare Beds because the Care-Lock feature may fail to stay engaged, posing a safety risk to patients.

    Product
    Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed is a device intended for medical purposes. The bed includes a built-in electric motor and remote controls that can be operated by the patient to adjust the height and surface contour of the bed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2693-2014·2014-10-01

    ArjoHuntleigh Recalls Minstrel Mobile Passive Hoists Due to Bolt Failure

    ArjoHuntleigh is recalling 18 Minstrel mobile passive hoists because a bolt under the scale may unscrew, posing a risk of the spreader bar detaching during use.

    Product
    Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult residents on horizontal floors in hospitals, nursing homes or other health care facilitates. The Minstrel device aids in the lifting, transfer and lowering to saf
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1451-2014·2014-04-16

    Harbor Freight Recalls Sit/Stand Rolling Walkers Due to Wheel Detachment Risk

    Harbor Freight Tools is recalling Sit/Stand Rolling Walkers because wheels may detach over time, posing a hazard to users.

    Product
    Sit/stand Rolling Walker, SKU/Item Number 66838. Intended for use by those with difficulty walking and weighing 225 lbs. or less.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1114-2014·2014-03-05

    Winco Premier Care Recliner 5570 Recalled for Lock Bar Defect

    Winco Mfg. is recalling 369 Premier Care Recliner 5570 units due to a manufacturing defect that may cause the lock bar to fail.

    Product
    PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered, OPTIONAL Heat or Heat & Massage, OPTIONAL LiquiCell. The products are a multi position recliners with a steel frame used primarily in long term care or convale
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0634-2014·2014-01-15

    Invacare Recalls Tracer IV Wheelchairs Due to Warped Wheels

    Invacare is recalling 227 Tracer IV wheelchairs in Michigan because the wheels were warped and wobbled when rolled.

    Product
    Tracer IV wheelchairs, Heavy duty manual wheel chair, 24" seat width, 450 lbs. weight capacity. Distributed by Invacare, Elyria, OH 44035 For transportation to accomplish necessary tasks of daily living in a home or community environment for the user.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0167-2014·2013-11-13

    Invacare Aquatec Ocean Mobile Shower and Toilet Commode Recall

    Invacare is recalling Aquatec Ocean mobile shower and toilet commodes because backrest cushion fixtures may unlatch in reclined or tilted positions.

    Product
    Aquatec Ocean VIP, Aquatec Ocean Dual-VIP, Aquatec Ocean E-VIP mobile shower and toilet commode with tilting function. Mobile shower and toilet commode with tilting function
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1597-2013·2013-07-03

    RF Technologies Recalls Code Alert Advanced 4-Way Care Solution Due to Firmware Error

    RF Technologies is recalling 167 Code Alert Advanced 4-Way Care Solution units because a firmware error may delay alarm transmission to the server.

    Product
    Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies. This product is used to alert caregivers when a patient at risk for falls is leaving a bed or chair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2013·2013-06-26

    Zimmer Patient Helper Bed Frame Adapter Assembly Recalled for Weak Welds

    Zimmer, Inc. is recalling 344 Patient Helper Bed Frame Adapter Assemblies because they may have a weak weld where the mounting bars attach to the tube.

    Product
    Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified medical professionals to adapt a patient helper to a hospital bed. The patient helper is used to aid and assist the patient's mobility within a hospital bed and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0628-2013·2013-01-09

    Stryker Medical Surgical Beds Recalled for Brake Ring Defect

    Stryker is recalling 9 Model 3002SEX and 3005S3EX medical surgical beds because brake rings may not meet specifications, negatively impacting holding force.

    Product
    Medical Surgical Bed, Model 3002SEX Medical Surgical Bed The S3" MedSurg Bed, is intended to support and transport patients within the Med/Surg and Critical Care hospital environments. The bed is typically used in pre-op, post-op and recovery areas of hospital facilities. The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2490-2012·2012-10-10

    Stanley Tabs Professional Monitor Recalled for Alarm Failure

    Stanley Security Solutions is recalling 176 Tabs Professional Monitor units because they may fail to sound an alarm, potentially increasing the risk of falls.

    Product
    Tabs Professional Monitor, without pull cord or wall bracket, Model 25025. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2489-2012·2012-10-10

    Stanley Tabs Professional Monitor Recalled for Alarm Failure

    Stanley Security Solutions is recalling 4,749 Tabs Professional Monitors because they may fail to sound an alarm, potentially increasing the risk of falls.

    Product
    Tabs Professional Monitor, without wall bracket, Model 25023. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2492-2012·2012-10-10

    Stanley Security Solutions Recalls Tabs Professional Voice + Monitor Devices

    Stanley Security Solutions is recalling 12,111 Tabs Professional Voice + Monitor units because the monitor may fail to sound an alarm.

    Product
    Tabs Professional Voice + Monitor, with wire bracket, Model 25223. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2488-2012·2012-10-10

    Stanley Tabs Professional Monitor Recalled for Alarm Failure

    Stanley Security Solutions is recalling 2,754 Tabs Professional Monitors because they may fail to sound an alarm, potentially increasing the risk of falls.

    Product
    Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2491-2012·2012-10-10

    Stanley Security Solutions Recalls Tabs Professional Voice + Monitor Units

    Stanley Security Solutions is recalling 4,148 Tabs Professional Voice + Monitor units because the monitor may fail to sound an alarm.

    Product
    Tabs Professional Voice + Monitor, includes one wall bracket, Model 25222. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2461-2012·2012-10-03

    Invacare Recalls I-Fit Shower Chairs Due to Quality and Adverse Event Data

    Invacare is voluntarily recalling 21,168 I-Fit Shower Chairs (Models 9780, 9781, 9781-1) based on returned units and adverse event reports.

    Product
    Invacare¿ I-Fit" Shower Chair (Models 9780, 9781, 9781-1), Invacare Corporation, Elyria, OH 44035. These shower chairs are designed for individuals who require seating support when bathing or showering and provide comfort and safety in the bathtub.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·05048·2004-11-16

    Bowflex Fitness Machines Recalled for Seat Pin and Bracket Failure

    The Nautilus Group recalled Bowflex Power Pro and Ultimate fitness machines because seat pins or brackets can break, causing sudden movement and fall risks.

    Product
    Bowflex Power Pro and Bowflex Ultimate Fitness Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide