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.

101–125 of 646

  • HighFDA (Devices)·Z-2135-2020·2020-06-03

    MOTek Medical Recalls Body Weight Support Light Due to Yoke Detachment Risk

    MOTek Medical is recalling 80 units of the Body Weight Support Light (Model RB011) because a manufacturing deviation may cause the yoke to detach from the cable guide.

    Product
    Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to facilitate functional gait training of subjects with gait and/or balance impairment by providing dynamic partial vertical unloading during walking on a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V247000·2020-05-01

    Mercedes-Benz Recalls G-Class Vehicles Due to Child Safety Lock Label Error

    Mercedes-Benz is recalling 2019-2020 G550 and G63 vehicles because the child safety lock symbol may indicate the incorrect status, posing a risk to unrestrained children.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G63, G 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2020·2020-04-15

    Firefly Child Seats Recalled Due to Broken Latches

    James Leckey Design Ltd is recalling Firefly child seats because of reports of broken latches.

    Product
    Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable bath seat for children aged 1-8, The GoTo Seat is a light-weight, portable, postural support seat for kids, aged between 1 and 8 with disabilities.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1632-2020·2020-04-08

    Merits E604 Pilot Navigator Stairlift Recalled Due to Pinion Gear Defect

    Merits Health Products is recalling 82 E604 Pilot Navigator Stairlifts because the pinion gear may disengage from the track, allowing the lift to slip or jolt.

    Product
    Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V168000·2020-03-20

    Terex Recalls 2009-2016 Aerial Devices Due to Lift Cylinder Defect

    Terex is recalling 2009-2016 TCX and SML aerial devices because lift cylinder rod eyes may fail, causing the boom to drift down and increasing injury risk.

    Product
    TEREX — TEREX TCX, SML
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1452-2020·2020-03-18

    ARJOHUNTLEIGH Recalls Concerto and Basic Shower Trolleys Due to Safety Catch Failure

    ARJOHUNTLEIGH is recalling 669 Concerto and Basic Shower Trolleys because a mechanical failure in the safety catch could cause the side support to open, posing a risk of patient falls and injuries.

    Product
    Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483], BAB1007-01 [(01)05055982796255], BAB1101-01 [(01)05055982787949], BAB1102-01 [(01)05055982796156], BAB1103-01 [UDI: (01)05055982796163], BAB1107-01…
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-1429-2020·2020-03-11

    Seca Baby Scale Cart Recalled Due to Wheel Detachment Risk

    Seca is recalling 254 baby scale carts because wheels can loosen and detach, causing the cart to tip over and potentially injure a baby.

    Product
    Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-0353-2020·2019-11-20

    Heritage Medical 2000 Vascular Beds Recalled for Sudden Head Drop Hazard

    Heritage Medical Products is recalling 167 2000 Vascular beds due to a potential for the head of the bed to drop suddenly while a patient is lying on it.

    Product
    2000 Vascular with 30 Degree option
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0166-2020·2019-10-30

    Rifton E-Pacer Powered Lift Device Recalled for Buckle Fatigue Failure

    Community Products, LLC is recalling 167 Rifton E-Pacer powered lift devices because a design change makes the load-bearing buckle springs susceptible to fatigue failure.

    Product
    Rifton E-Pacer, SKU K660, powered lift device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19192·2019-08-29

    Decathlon Recalls Rocky Screwgate Carabiners Due to Unlocking Risk

    Decathlon USA is recalling about 50 Rocky Screwgate carabiners because incorrect assembly can cause them to unlock while in use, posing a risk of serious injury or death.

    Product
    Rocky Screwgate carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2294-2019·2019-08-28

    TiSport Recalls TiLite Wheelchair Anti-Tip Tubes for Tipping Risk

    TiSport is recalling 1,452 TiLite wheelchairs because the anti-tip tubes may fail, allowing the chair to tip backwards.

    Product
    TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19167·2019-07-16

    VIVO Recalls Speaker Wall Mounts Due to Fall and Injury Hazards

    VIVO is recalling MOUNT-PLAY5 speaker wall mounts because the front ledge can loosen, causing speakers to fall. No injuries have been reported.

    Product
    VIVO MOUNT-PLAY5 speaker wall mounts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V511000·2019-07-02

    Nova Bus Recalls 2014-2017 LFS Models Due to Seat Hardware Defect

    Nova Bus is recalling 2014-2017 LFS and LFS Artic buses because improperly tightened seat hardware may cause cantilever seats to drop, increasing injury risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1351-2019·2019-05-22

    Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk

    Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.

    Product
    Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1352-2019·2019-05-22

    Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk

    Moller Vital is recalling Molift 2-Point sling bars because broken hooks may cause the sling to slip and patients to fall.

    Product
    Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001 1830002 1830002C 1830003
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·19V357000·2019-05-13

    Lance Camper Recalls 2019-2020 Truck Campers Due to Bunk Bed Gap

    Lance Camper is recalling 2019-2020 855S and 1172 Truck Campers because a gap in the fold-down bunk bed may allow occupants to fall and get stuck.

    Product
    LANCE CAMPER — LANCE CAMPER TRUCK CAMPER (855S), TRUCK CAMPER (1172)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V271000·2019-04-03

    Ford E-150 and Transit Vans Recalled for Wheelchair Lift Defect

    Mobility Specialists is recalling 2014-2017 Ford E-150 and Transit vans with wheelchair lifts that may fail, posing a tipping risk to users.

    Product
    FORD — FORD, MOBILITY SPECIALISTS E-150, TRANSIT, FORD E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V198000·2019-03-13

    TCI Recalls 2015 and 2017 Transtech Buses with Wheelchair Lift Defect

    Transportation Collaborative is recalling 2015 and 2017 Transtech buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    TRANS TECH — TRANS TECH CST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V160000·2019-03-01

    Supreme Classic American Trolley Recall for Wheelchair Lift Defect

    Supreme is recalling 2014-2016 Classic American Trolley vehicles because a wheelchair lift cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    SUPREME — SUPREME CLASSIC AMERICAN TROLLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V158000·2019-03-01

    Ameritrans Recalls One 2016 E225 Bus Due to Wheelchair Lift Defect

    Ameritrans is recalling one 2016 E225 bus because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    AMERITRANS — AMERITRANS E225
    Category
    Vehicle
    Distribution
    Distributed nationwide