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.

126–150 of 646

  • HighNHTSA·19V140000·2019-02-27

    Midway Recalls One 2016 Freightliner Sprinter 3500 Wheelchair Lift Vehicle

    Midway Specialty Vehicles is recalling one 2016 Freightliner Sprinter 3500 because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V125000·2019-02-26

    Ford E-250 wheelchair lift cam failure recall

    New England Wheels is recalling 2008, 2013, and 2014 Ford E-250 vans with Ricon wheelchair lifts because the positioning cam may fail, causing the platform to rise too high.

    Product
    FORD — FORD E-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V116000·2019-02-21

    Winnebago Metro Link Recall for Wheelchair Lift Cam Failure

    Winnebago is recalling 2014 Metro Link vehicles because a wheelchair lift cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    WINNEBAGO — WINNEBAGO METRO LINK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0824-2019·2019-02-20

    Steris ATLAS Loading Car Recalled for Latch Failure Risk

    Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.

    Product
    ATLAS Loading Car
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V102000·2019-02-15

    Goshen Shuttle Buses Recalled for Wheelchair Lift Cam Failure

    Eldorado is recalling 2012-2018 Goshen shuttle buses because a wheelchair lift cam may fail, allowing the platform to rise too high and risk injury.

    Product
    GOSHEN — GOSHEN GCII, IMPULSE, PACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V081000·2019-02-11

    Blue Bird Recalls One 2019 Vision Bus for Wheelchair Lift Defect

    Blue Bird is recalling one 2019 Vision bus because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V082000·2019-02-11

    Blue Bird Recalls School Buses with Defective Wheelchair Lifts

    Blue Bird is recalling 2015-2019 Vision and All American school buses because a wheelchair lift component may fail, causing the platform to rise too high and increasing the risk of injury.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0589-2019·2018-12-19

    Arjo Passive Clip Sling Recalled for Material Breakage Risk

    ArjoHuntleigh is recalling 10 units of Passive Clip Slings because the material may break during patient transfers, posing a risk of falls and serious injury.

    Product
    ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo Passive Clip Sling is a product intended for assisted transfer of patient/resident with limited ability to move. Designed to be used for one patient during hospital stay and assists the caregiver…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0105-2019·2018-10-24

    Liko Multirall 200Liko Strap Gripper Overhead Lift Recall

    Liko AB is recalling two Multirall 200Liko Strap Gripper overhead lifts due to potential assembly errors that could cause patient falls.

    Product
    Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·18V706000·2018-10-09

    Altec Recalls Aerial Devices and Digger Derricks Due to Step Defect

    Altec is recalling 2017-2018 aerial devices and digger derricks because a step on the fiberglass platform can break off, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3178-2018·2018-09-26

    Permobil Recalls Powered Wheelchairs Due to Backrest Bar Failure Risk

    Permobil is recalling 3,134 powered wheelchairs because backrest support bars may fail, potentially causing users to fall backward and sustain injuries.

    Product
    Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V640000·2018-09-18

    Forest River Recalls Buses with Defective Wheelchair Lifts

    Forest River is recalling specific 2012-2018 buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELKHART, GLAVAL BUS ALLSTAR XL MVP, ALLSTAR, SENATOR II, STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2962-2018·2018-09-12

    Bayer Medical Care Recalls Overhead Counterpoise Systems Due to Structural Risk

    Bayer Medical Care is recalling four Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS, 580mm CEILING MOUNT, PORTEGRA2, Catalog # OCS CEIL 58, Material Number 84433765
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2960-2018·2018-09-12

    Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure

    Bayer Medical Care is recalling two Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253
    Category
    Medical Device
    Distribution
    3 states
  • HighNHTSA·18V611000·2018-09-11

    Coach and Equipment Transit Buses Recalled for Wheelchair Lift Defect

    Coach and Equipment is recalling certain transit buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METRO LITE, CONDOR LT, PEGASUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V603000·2018-09-10

    Turtle Top Transit Buses Recalled for Wheelchair Lift Cam Failure

    Turtle Top is recalling 2013-2018 Odyssey, VanTerra, and Terra Transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, ODYSSEY, TERRA TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V584000·2018-09-04

    Collins School Bus Recall for Wheelchair Lift Cam Failure

    Collins Bus is recalling 2012-2018 school buses with Ricon wheelchair lifts because a cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    COLLINS — COLLINS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V583000·2018-08-31

    Eldorado Transit Bus Recall for Wheelchair Lift Cam Failure

    Eldorado is recalling 2012-2018 transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    ELDORADO — ELDORADO, GOSHEN AERO ELITE, AEROTECH, IMPULSE, TRANSTECH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V574000·2018-08-30

    Micro Bird School Bus Wheelchair Lift Cam Recall

    Micro Bird is recalling 2012-2018 school buses with specific wheelchair lifts because a cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 SCHOOL BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V573000·2018-08-30

    Champion Recalls Buses with Defective Wheelchair Lifts

    Champion is recalling 2012-2018 buses with specific wheelchair lifts where a cam may fail, allowing the platform to rise too high and risk injury.

    Product
    CHAMPION — CHAMPION DEFENDER, AMERICAN CRUSADER, AMERICAN COACH, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2753-2018·2018-08-29

    Handicare P600 Series Patient Lift Recalled for Strap Wear and Breakage

    Handicare USA Inc. is recalling four P600 Series patient lifts due to premature strap wear and breakage at maximum weight conditions.

    Product
    Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2752-2018·2018-08-29

    Handicare C Series Patient Lifts Recalled for Premature Strap Wear

    Handicare USA Inc. is recalling 716 C Series Patient Lifts because straps may wear and break prematurely at maximum weight conditions.

    Product
    Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V563000·2018-08-24

    Navistar Recalls 2015-2019 IC Bus School Buses Due to Wheelchair Lift Defect

    Navistar is recalling 2015-2019 IC Bus school buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    IC BUS — IC BUS CESB, CASB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V560000·2018-08-23

    Thomas Built Buses Recalling Wheelchair Lifts Due to Cam Failure

    Daimler Trucks is recalling 2015-2019 Thomas Built Buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide