The Recall Desk

Hazard

Fall Injury recalls

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

What the numbers show

Total
641
Critical
9
Severe
144
Most recent
2026-08-20

Of the 641 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 144 (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.

301–325 of 641

  • SevereFDA (Devices)·Z-1461-2014·2014-04-23

    Philips CT Scanners Recalled for Defective Service Latch Component

    Philips Medical Systems is recalling 135 CT scanners because a defective service latch component can cause the patient table top to become free-floating.

    Product
    Brilliance CT 16, Brilliance CT 64, Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology, Brilliance iCT, Ingenuity CT, Ingenuity Core, Ingenuity Core 128 and Ingenuity Flex scanners are Computed Tomography X-ray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V216000·2014-04-23

    Ford E-350 wheelchair lift roll stop latch recall

    Advanced Wheels is recalling 2008-2010 Ford E-350 vans with wheelchair lifts due to bent or misaligned roll stop latches that could allow occupants to fall.

    Product
    FORD — FORD E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2014·2014-04-16

    Medcare Floor Lifts Recalled Due to Potential Pin Failure

    ErgoSafe Product LLC is recalling Medcare Floor Lifts manufactured between 2010 and 2012 because a design pin may break over time.

    Product
    400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The intended use is a patient hanger bar (400600) attached to a 400003 or 400013 floor lift used to lift, transfer or position clients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V197000·2014-04-16

    Cummings recalls wheelchair lifts on Ford and Chevrolet vans

    Cummings Mobility is recalling wheelchair lifts on certain Ford and Chevrolet vans because roll stop latches may bend, posing a fall risk.

    Product
    FORD — FORD, CHEVROLET E-350, C5500, G3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V122000·2014-03-13

    Terex Recalls 2014 TZ-50 Aerial Work Platforms Due to Weld Defects

    Terex is recalling 2014 TZ-50 trailer-mounted aerial work platforms because a welding process change may cause cracks in the boom section, risking platform failure.

    Product
    TEREX — TEREX TZ-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2014·2013-12-11

    Sunrise Zippie Voyage Stroller Recalled for Potential Seat Dislodgement

    Sunrise Medical is recalling Zippie Voyage strollers because a plastic latch may deform, allowing the seat to dislodge and causing the occupant to slide out.

    Product
    Sunrise Brand Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), Model: EIZ14; Product is manufactured and distributed by Sunrise Medical (US) LLC., Fresno, CA. Used by a person to move from one place to another while sitting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0370-2014·2013-11-27

    FDA Recalls Medcare Max-500 Patient Lifts Due to Potential Load Failure

    Ergosafe Products LLC is recalling 97 Medcare Max-500 patient stands because the lift might fail with the labeled 500-lb load rating.

    Product
    Medcare Products Max-500 Stand, Total Support, patient stand, model #400006. The responsible firm name listed in the Operations Manual is Medcare Products, Burnsville, MN. Used for assisting patients/residents to a standing position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0363-2014·2013-11-27

    Stryker Rose Bed Siderail Latch Failure Recall

    Stryker is recalling Model FL14E Rose Beds because siderails may appear latched when they are not, posing a risk of patient injury.

    Product
    Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that consists of a bed with a built-in motor and controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and lat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0371-2014·2013-11-27

    FDA Recalls Medcare Max-500 Patient Stands Due to Load Failure Risk

    Ergosafe Products LLC is recalling 233 Medcare Max-500 patient stands because the lift mechanism might fail under the labeled 500-lb load rating.

    Product
    Medcare Products Max-500 Stand-N-Weigh, Total Support, patient stand, model #400007. The responsible firm name listed in the Operations Manual is Medcare Products, Burnsville, MN. Used for assisting patients/residents to a standing position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V417000·2013-09-12

    Terex Recalls XT55 and XT60 Aerial Devices Due to Boom Cracks

    Terex is recalling 1997-2013 XT55 and XT60 aerial devices because cracks in the boom hinge may cause the platform to fall, risking injury.

    Product
    TEREX — TEREX XT60, XT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1807-2013·2013-07-31

    Etac Swift Mobil Shower Chairs Recalled for Stability Risk

    Etac is voluntarily recalling Swift Mobil shower chairs because a lost caster can cause instant instability and potential injury.

    Product
    Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt shower chair. Height adjustable four wheeled shower chairs for persons of various weights.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1794-2013·2013-07-31

    Hill-Rom TotalCare Bed Recall Due to Mattress Egress Injury Risk

    Hill-Rom is recalling 4,121 TotalCare Beds because the mattress may not stay flat in the chair egress position, creating a risk of patients falling or sliding to the floor.

    Product
    TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum Complete mattress, and AccuMax Quantum Convertible mattress The TotalCare Bed System is intended to provide a patient support ideally suited to be used in health care environments. The TotalCare Bed System m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1466-2013·2013-06-12

    Hill-Rom 1000 Hospital Bed Recalled Due to Brake Disengagement Risk

    Hill-Rom, Inc. is recalling 8,737 Hill-Rom 1000 Beds because brakes may disengage when the bed frame is subjected to a hard jolt or force.

    Product
    Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medical surgical area of the hospital.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1480-2013·2013-06-12

    Kreg Medical Recalls E-Z Wider Bariatric Chair Beds Due to Collapse

    Kreg Medical Inc. is recalling 59 E-Z Wider Bariatric Chair Beds because the bed frame collapsed during patient use, leaving the patient in a forward tilt position.

    Product
    E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13E033000·2013-06-07

    Kuryakyn Recalls Motorcycle Backrests Due to Loose Pivot Screws

    Kuryakyn is recalling specific motorcycle backrests because pivot screws may loosen, causing the backrest to separate and potentially leading to loss of control.

    Product
    SEATS:MOTORCYCLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1128-2013·2013-04-24

    SR Instruments FG3105 Patient Scales Recalled Due to Load Cell Failures

    SR Instruments is recalling 806 FG3105 patient scales used with Joerns Healthcare lifters after two load cell failures caused patient falls.

    Product
    SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare Patient Lifters. Model# FG3105 Patient Scales. Product Usage: The FG3105 Scale is designed for Joerns Healthcare for use in portable patient weighing systems. The scale is designed to be connected betwe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2013·2013-03-06

    Philips MX 16-Slice CT Scanner Recall Due to Loose Table Screws

    Philips Medical Systems is recalling 412 MX 16-Slice CT Scanner Systems because loose screws may cause the patient table top to detach.

    Product
    Philips MX 16-Slice CT Scanner System, a whole-body computed tomography X-ray system.
    Category
    Medical Device
    Distribution
    18 states
  • SevereFDA (Devices)·Z-0872-2013·2013-02-27

    Hill-Rom Recalls Liko Overhead Rail Systems Due to Corrosion

    Hill-Rom is recalling Liko Overhead Rail Systems because hardware corrosion in high-humidity areas caused two rail failures.

    Product
    Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and Masterlift Systems Product Usage - The Overhead Rail System allows overhead lifts to be mounted to the ceiling allowing versatility for use in lifting situ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V062000·2013-02-25

    Pierce Recalls 2007-2010 Velocity and Impel Fire Trucks for Door Defect

    Pierce Manufacturing is recalling 2007-2010 Velocity and Impel fire trucks because inner door handle springs may allow doors to open inadvertently while in motion.

    Product
    PIERCE — PIERCE VELOCITY, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13107·2013-01-30

    Sportspower BouncePro 14' Trampolines Recalled for Fall Hazard

    Sportspower is expanding a recall of BouncePro 14' trampolines sold at Walmart because the enclosure netting can break, posing a fall hazard.

    Product
    Sportspower BouncePro 14' Trampolines
    Category
    Consumer Product
    Distribution
    Distributed nationwide