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.

176–200 of 641

  • HighFDA (Devices)·Z-0942-2017·2017-01-11

    Pride Mobility Recalls TRU-Balance 3 Power Positioning Systems

    Pride Mobility Products Corp is recalling 12,343 TRU-Balance 3 Power Positioning Systems because the back and tilt base can separate when tilted beyond the specified angle.

    Product
    TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0928-2017·2017-01-04

    Allen Medical Systems Recalls Arthex S3 Arm Sleeve Connectors

    Allen Medical Systems is recalling 420 Arthex S3 Arm Sleeve Connectors because they may separate unexpectedly during use, potentially causing moderate injury to patients.

    Product
    Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0732-2017·2016-12-21

    GF Health Products Recalls Patriot Homecare Beds Due to Motor Defect

    GF Health Products is voluntarily correcting Patriot homecare beds because contaminated motor housings may crack, potentially causing the head section to fall.

    Product
    Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3 Head/Foot Motors. Description Part Number Motor and Pendant Patriot Full Electric 120V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V905000·2016-12-15

    Jayco Recalls 2016 Alante and Precept Motorhomes for Step Wiring Defect

    Jayco is recalling 2016 Alante and Precept motorhomes because incorrectly installed entrance step wiring may cause the steps to retract unexpectedly, posing a fall risk.

    Product
    JAYCO — JAYCO ALANTE, PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0326-2017·2016-11-09

    Hill-Rom Recalls Ceiling Brackets Due to Potential Fall Hazard

    Hill-Rom is recalling 188 ceiling brackets with a larger center hole that could cause the system to fall if the safe working load is exceeded.

    Product
    Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·16V768000·2016-10-21

    Newmar Recalls 2017 Motorhomes Due to Hydraulic Step Retraction Risk

    Newmar is recalling 2017 King Aire, Essex, and London Aire motorhomes because the hydraulic entry step controller may allow steps to retract unexpectedly, increasing the risk of injury.

    Product
    NEWMAR — NEWMAR LONDON AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0040-2017·2016-10-12

    Trumpf Medical Systems Recalls TruSystem Mobile Operating Columns

    Trumpf Medical Systems is recalling 84 TruSystem mobile operating columns because they may unexpectedly descend approximately 20 centimeters.

    Product
    Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem 5500, Material Number 1607822 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0013-2017·2016-10-12

    Siemens Recalls Multix Fusion X-Ray Systems Due to Table Tilt Risk

    Siemens is recalling 37 Multix Fusion X-ray systems because an internal table part may detach, causing the table to tilt and potentially injure patients.

    Product
    Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including: skull, chest, abdomen and extremities and may be
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16E076000·2016-09-29

    Thieman Liftgates Recalled for Potential Roller Chain Failure

    Thieman is recalling specific liftgates because roller chains may fail, causing the platform to drop and increasing injury risk.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2718-2016·2016-09-14

    ArjoHuntleigh Sara Combilizer Recalled for Potential Tipping Hazard

    ArjoHuntleigh is recalling 106 Sara Combilizer patient lifts due to a potential tipping hazard identified during internal testing. No adverse events or customer complaints have been reported to date.

    Product
    ArjoHuntleigh Sara Combilizer; Intended to facilitate early immobilization, rehabilitation, and care of patients.
    Category
    Medical Device
    Distribution
    13 states
  • HighNHTSA·16V633000·2016-08-31

    Peterbilt 567 Truck Recalled for Tripping Hazard on Left Rail

    PACCAR is recalling one 2017 Peterbilt 567 truck because a bracket protrudes upward, creating a tripping hazard. Dealers will move the connections to the right rail free of charge.

    Product
    PETERBILT — PETERBILT 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2376-2016·2016-08-17

    Hill-Rom Recalls Volker Series Hospital Beds Due to Side Rail Defect

    Hill-Rom is recalling Volker 2080, 2082, S 280, and S 282 series hospital beds because the side rail latch may fail, causing the rail to lower and the patient to fall.

    Product
    Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Product Usage: Volker model 2080/3010/3080 nursing beds are intended for the care of residents in rooms in nursing homes, in residential homes for the elderly and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2331-2016·2016-08-10

    Stryker Recalls Spirit Plus Hospital Beds Due to Actuator Failure

    Stryker Medical is voluntarily recalling Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.

    Product
    Spirit Plus Bed, A-C Powered Hospital Bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2291-2016·2016-08-03

    Moller Vital Molift Air Ceiling Hoist Recall for Loose Bolt Risk

    Moller Vital is recalling Molift Air ceiling hoists because the suspension coupling bolt may come loose, posing a risk of patient falls.

    Product
    Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300, Molift Air 300 Propulsion, Molift Air 300 IRC, Molift Air 300 IRC Propulsion Molift Air is a ceiling hoist used to lift and transfer immobilized patients in various situatio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2102-2016·2016-07-06

    Medical Depot Recalls EZ Adjust Aluminum Crutches Due to Tip Failure

    Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches because the tip may fail, posing a risk of injury.

    Product
    EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ ad
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2101-2016·2016-07-06

    Medical Depot Recalls Aluminum Crutches Due to Tip Failure

    Medical Depot Inc. is recalling 123,125 pairs of aluminum crutches nationwide because the metal tip may fail. Users should stop using the product.

    Product
    Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum crut
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V477000·2016-06-28

    Terex Recalls 2015-2016 Aerial Devices Due to Platform Tilt Risk

    Terex is recalling 2015-2016 HR, HRX, TC, and TCX aerial devices because poor welds on the platform leveling cylinder may cause the platform to tilt, risking occupant falls.

    Product
    TEREX — TEREX HRX, HR, TC, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V464000·2016-06-24

    Volkswagen Recalls 2016 Models for Rear Child Door Lock Defect

    Volkswagen is recalling 2016 CC, Golf R, Tiguan, and e-Golf vehicles because vibrations may cause rear child door locks to disengage, allowing children to open doors.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, GOLF R, CC, E-GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1916-2016·2016-06-15

    Hill-Rom Recalls Liko Universal SlingBars Due to Center Bolt Failure Risk

    Hill-Rom is recalling Liko Universal SlingBars because the center bolt may weaken and break, posing a risk of patient falls and injury.

    Product
    Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Universal SlingBar" 450, Universal SlingBar" 450 QRH, Universal SlingBar" 450 R2R, Universal SlingBar" 600 Universal SlingBar" 600 QRH Component of Liko
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16164·2016-05-19

    Black Diamond Recalls Index Climbing Ascenders Due to Fall Hazard

    Black Diamond is recalling Index Ascenders because a rivet may release, causing the device to detach from the rope and posing a risk of injury or death.

    Product
    Black Diamond Index Ascenders for climbing
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V317000·2016-05-18

    Mobility Works Recalls Vans with Defective Ricon Wheelchair Lifts

    Mobility Works is recalling 2014-2015 Ford and Chevrolet vans equipped with specific Ricon wheelchair lifts due to a risk of platform separation and injury.

    Product
    MOBILITY WORKS — MOBILITY WORKS CHEVY EXPRESS 2500, FORD E-150, FORD E-250, FORD E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1530-2016·2016-04-27

    Acorn 180 Curved Stairlift Recalled Due to Broken Rivets

    Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.

    Product
    Acorn 180 Curved Stairlift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16143·2016-04-14

    Fisher-Price Recalls Infant Cradle Swings Due to Fall Hazard

    Fisher-Price is recalling about 34,000 infant cradle swings because the seat peg may not be fully engaged, allowing the seat to fall unexpectedly.

    Product
    Cradle 'n Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V180000·2016-03-30

    Starcraft RV Recalls 2016 Launch Ultra Lite Trailers Due to Step Defect

    Starcraft RV is recalling 26 model year 2016 Launch Ultra Lite trailers because entry steps may have been installed with improper bolts, posing a fall risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide