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.

226–250 of 641

  • HighFDA (Devices)·Z-2467-2015·2015-09-02

    Sunrise Medical Recalls Quickie IRIS Wheelchairs with Dynamic Backrest

    Sunrise Medical is recalling 64 Quickie IRIS wheelchairs because the backrest system may break, posing a risk of falls or injury to the occupant.

    Product
    Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code 183M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2461-2015·2015-09-02

    Ferno iNX Wheeled Stretcher Wheel Caster Set Screw Recall

    Ferno-Washington Inc is recalling 26 Ferno iNX Wheeled Stretchers due to improperly installed wheel caster set screws that may allow bearing cups to back out.

    Product
    Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.
    Category
    Medical Device
    Distribution
    7 states
  • HighNHTSA·15V531000·2015-08-19

    Thor Motor Coach Recalls Tuscany XTE Motorhomes for Table Defect

    Thor Motor Coach is recalling 2014-2015 Tuscany XTE motorhomes because the dinette table insert may flip up if sat on, posing a fall risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY XTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2270-2015·2015-08-05

    Prism Medical P-600 Portable Ceiling Lift Recalled for Sling Attachment Risk

    Prism Medical is recalling 409 P-600 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.

    Product
    Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 lbs (273 kg). Product Usage: The P-600 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2269-2015·2015-08-05

    Prism Medical P-440 Portable Ceiling Lift Recalled for Sling Attachment Risk

    Prism Medical is recalling P-440 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.

    Product
    Prism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weight specification of 440 lbs (200 kg). Product Usage: The P-440 lift is a lifting aid used by health care professionals and those providing care in the home to lift, positi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2073-2015·2015-07-22

    Etac Supporter toilet armrest recalled due to loose fasteners

    Etac Supply Center Ab is recalling 25 units of Supporter toilet armrests because fasteners may come loose, causing the product to become unsteady.

    Product
    Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfortable rounded grips for the hands. Supporter is simple to mount without the need for any tools. It fits both floor and wall mounted toilets. If space around the toilet is limited either armr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2015·2015-07-15

    BTE Technologies Recalls Primus Exercise Devices Due to Detachment Risk

    BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.

    Product
    Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque resistance to patient motion during rehabilitation therapy. The Primus that includes the optional Chop / Lift Bar.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1818-2015·2015-06-24

    Hill-Rom Viking Mobile Patient Lifts Recalled for Potential Free Fall Hazard

    Hill-Rom is recalling Viking M, L, and XL Mobile Lifts because a damaged actuator can cause the lift arm to drop suddenly, posing a risk of patient injury or death.

    Product
    Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·15V377000·2015-06-16

    EverGreen Recalls Fifth Wheel Trailers Due to Step Rivet Failure Risk

    EverGreen is recalling 2014-2016 fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to give and increasing the risk of injury.

    Product
    EVERGREEN — EVERGREEN LIFESTYLE, ALPHA GOLD, BAY HILL, TESLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V374000·2015-06-15

    New Horizons Recalls 2013-2015 Summit and Majestic RVs for Step Defect

    New Horizons is recalling 2013-2015 Summit and Majestic RVs because a rivet on the quad entry steps may fail, causing the steps to give and increasing the risk of injury.

    Product
    NEW HORIZONS — NEW HORIZONS MAJESTIC, SUMMIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V356000·2015-06-09

    Gulf Stream Recalls 2015 Trailers Due to Failing Entry Step Rivets

    Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.

    Product
    GULF STREAM — GULF STREAM CANYON TRAIL, SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1650-2015·2015-06-03

    Philips Brilliance CT 40 Recalled Due to Unexpected Couch Descent

    Philips Medical Systems is recalling 153 Brilliance CT 40 systems because the patient couch may unexpectedly descend to its lowest point during an exam.

    Product
    Brilliance CT 40. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1649-2015·2015-06-03

    Philips Brilliance CT 64 Systems Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 64 systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 64. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1655-2015·2015-06-03

    Philips Brilliance CT 6 Air Systems Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 6 Air systems because the patient couch unexpectedly descended during exams. The units were distributed in China.

    Product
    Brilliance CT 6 Air. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1657-2015·2015-06-03

    Philips Ingenuity CT Recall for Unexpected Patient Couch Descent

    Philips is recalling 153 Ingenuity CT systems in China because the patient couch unexpectedly descended to its lowest point during an exam.

    Product
    Ingenuity CT. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1647-2015·2015-06-03

    Philips MX8000 CT Scanner Recall Due to Unexpected Couch Descent

    Philips is recalling 153 MX8000 CT scanners because the patient couch may descend unexpectedly during an exam.

    Product
    MX8000 Dualv. EXP, 728130. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1652-2015·2015-06-03

    Philips Brilliance CT 16 Water Computed Tomography Systems Recalled for Couch Descent

    Philips Medical Systems is recalling 153 Brilliance CT 16 Water systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 16 Water. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1653-2015·2015-06-03

    Philips Brilliance CT 16 Air Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 16 Air systems because the patient couch may unexpectedly descend to its lowest point during an exam.

    Product
    Brilliance CT 16 Air. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1651-2015·2015-06-03

    Philips Brilliance CT 16 Power Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 16 Power systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 16 Power. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1654-2015·2015-06-03

    Philips Brilliance CT 10 Air Recalled for Unexpected Couch Descent

    Philips Medical Systems is recalling 153 Brilliance CT 10 Air systems in China because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 10 Air. Computed Tomography X-ray systems 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
    0 states
  • HighFDA (Devices)·Z-1656-2015·2015-06-03

    Philips Brilliance iCT CT Systems Recalled for Unexpected Couch Descent

    Philips Medical Systems is recalling 153 Brilliance iCT computed tomography systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance iCT. Computed Tomography X-ray systems 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
    0 states
  • HighNHTSA·15V308000·2015-05-26

    Open Range Recalls 2015 Fifth Wheel Trailers Due to Step Rivet Failure

    Open Range R.V. Company is recalling 122 model year 2015 Roamer, Mesa Ridge, and 3X fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to fail.

    Product
    OPEN RANGE — OPEN RANGE 3X, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V304000·2015-05-22

    Highland Ridge RV Recalls 2015 Fifth Wheel Trailers Due to Step Rivet Failure

    Highland Ridge RV is recalling 2015 Roamer and Mesa Ridge fifth wheel trailers because a rivet on the quad entry steps may shear, causing the steps to give and increasing the risk of injury.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT MESA RIDGE, ROAMER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V273000·2015-05-11

    Forest River Recalls Trailers Due to Failing Entry Step Rivets

    Forest River is recalling specific 2013-2015 RV trailers because a rivet on the quad entry steps may shear, causing the steps to fail and increasing the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK, DYNAMAX, SIERRA, CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V266000·2015-05-07

    Jayco Recalls 2013-2015 Trailers Due to Failing Entry Step Rivets

    Jayco is recalling 2,747 model year 2013-2015 Seismic and Eagle Premier trailers because entry step rivets may shear, causing steps to fail and occupants to fall.

    Product
    JAYCO — JAYCO, JAYCO FIFTH WHEEL SEISMIC, EAGLE PREMIER
    Category
    Vehicle
    Distribution
    Distributed nationwide