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.

251–275 of 641

  • HighNHTSA·15V198000·2015-04-03

    Heartland Recalls 2015 Trailers Due to Step Rivet Failure Risk

    Heartland is recalling 2015 fifth wheel and travel trailers because a rivet on the quad entry steps may shear, causing the steps to fail and increasing the risk of injury.

    Product
    HEARTLAND — HEARTLAND ELKRIDGE, ROAD WARRIOR, LANDMARK 365, BIGHORN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1288-2015·2015-03-25

    Ossur LP Rotate Foot System Recalled for Insecure Assembly

    Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.

    Product
    LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid adapte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V173000·2015-03-24

    KZ-RV Recalls 723 Recreational Vehicles Due to Failing Entry Step Rivets

    KZ-RV is recalling 723 recreational vehicles because a rivet on the quad entry steps may shear and fail, causing the steps to give and increasing the risk of personal injury.

    Product
    KZ-RV — KZ-RV STONERIDGE, GOLD, PRESTIGE, GOLDRUSH NUGGET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V112000·2015-02-25

    Farber Specialty Vehicles Recalls Wheelchair Lifts Due to Cracking Risk

    Farber Specialty Vehicles is recalling specialty vehicles equipped with Ricon wheelchair lifts because the platform side plates may crack, posing a risk of injury.

    Product
    WINNEBAGO — WINNEBAGO, FREIGHTLINER, FORD WFJ33S, MBC, XCS, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V102000·2015-02-23

    Keystone Recalls 2013-2015 RVs Due to Failing Entry Step Rivets

    Keystone RV Company is recalling 5,390 Montana, Raptor, and Dutchmen Voltage vehicles because entry step rivets may shear, causing the steps to fail and increasing the risk of falls.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN RAPTOR, MONTANA, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E010000·2015-02-18

    Gillig Recalls S5510 Wheelchair Lifts Due to Platform Cracking Risk

    Gillig LLC is recalling S5510 series wheelchair lifts manufactured by Ricon Corporation between November 2010 and February 2011. The platform side plates may crack, posing a risk of injury if the platform falls.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0995-2015·2015-01-28

    Ferno Model 35X Stretchers Recalled Due to Loose Wheel Assemblies

    Ferno-Washington Inc is recalling 46 Model 35X stretchers because wheel castor assemblies may loosen, posing a risk of injury.

    Product
    Ferno Model 35X PROFlexx Stretchers, one unit per package
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-1003-2015·2015-01-28

    Dick's Sporting Goods Recalls Fitness Gear Inversion Tables Due to Injury Reports

    Dick's Sporting Goods is recalling Fitness Gear Inversion Tables because customers reported falling and sustaining injuries. The products were distributed nationwide.

    Product
    Fitness Gear Inversion table (Style STE00059FG or Style STE00118FG), Distributed by ASLI, Wilmington, DE (on carton), Paradigm Health & Wellness, Inc. (in user manuals); The products are inversion tables, which allow the user to secure his or her ankles to the table and invert.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15063·2015-01-22

    Primal Vantage Recalls Ameristep Hyde Tree Stands Due to Fall Hazard

    Primal Vantage is recalling about 1,000 Ameristep Hyde tree stands because the aluminum platform can break, posing a fall risk to hunters.

    Product
    Ameristep Hyde Cliff Hanger and Sky Walker Tree Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V825000·2014-12-29

    Dodgen Recalls Mobility RVs Due to Wheelchair Lift Platform Cracking Risk

    Dodgen is recalling 2006-2014 Mobile Tech. Mobility RVs equipped with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    DODGEN — DODGEN MOBILE TECH. MOBILITY RV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0523-2015·2014-12-17

    Siemens Mammomat Inspiration System Recalled for Potential Instability

    Siemens is recalling three Mammomat Inspiration systems because the workstation table may fall over if not secured, posing a risk of serious injury.

    Product
    Mammomat Inspiration system: Product Usage: mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be interpreted by either hard copy film or soft copy workstation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V799000·2014-12-17

    Winnebago WFG38S Recalled for Wheelchair Lift Platform Cracking Risk

    Farber Specialty Vehicles is recalling 2005-2008 Winnebago WFG38S vehicles with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    WINNEBAGO — WINNEBAGO WFG38S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15046·2014-12-10

    GCI Outdoor Recalls Stadium Seats Due to Backrest Failure Risk

    GCI Outdoor is recalling about 6,000 BleacherBack stadium seats because the backrest can fail, posing a risk of injury. Consumers should stop using the seats and contact the company for a repair kit.

    Product
    Stadium seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V742000·2014-11-19

    Champion Transit Buses Recalled for Wheelchair Lift Platform Cracking Risk

    Champion Bus is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    CHAMPION — CHAMPION HCAC, STACKED RAIL, PLATINUM SHUTTLE, DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2015·2014-11-19

    Roscoe Medical Recalls Transport Rollators Due to Caster Separation Risk

    Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.

    Product
    Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down footrests, ergonomic handles, curved padded backrest and handy wire basket for storage. Item# 30192 Burgundy each/Item# 30194 Blue each.. Transport Rollator is a whee
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V729000·2014-11-13

    Starcraft Bus Recalls Transit Buses Due to Wheelchair Lift Defect

    Forest River is recalling 2006-2012 Starcraft transit buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS STARQUEST, ULTRASTAR, ALLSTAR, XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V718000·2014-11-10

    Sutphen Aerial Devices Recalled for Potential Ladder Cable Failure

    Sutphen is recalling 2000-2014 aerial devices because a cable failure could cause the ladder to collapse, increasing injury risk.

    Product
    SUTPHEN — SUTPHEN SPI 112, SAI 110, SPH 100, SP 110
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0142-2015·2014-11-05

    Mabis Recalls DMI Rollator Transport Chairs Due to Collapse Risk

    Briggs Medical Service Company is recalling 1,869 DMI Rollator Transport Chairs because they may collapse during use.

    Product
    DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4"; Seat Size: 14" x 12 3/4"; Handle Height: 31" - 36"; Width Between Handles: 18"; Weight: 19 Lbs; Walking assistance device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0079-2015·2014-10-22

    ArjoHuntleigh Recalls Spreader Bars for Ceiling Lifts Due to Hook Flexibility

    Arjo, Inc. is recalling 363 spreader bars for the Maxi Sky 2 Ceiling Lift because the hooks are too flexible to securely hold sling loops.

    Product
    Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Model 700-19425. Intended to be used for general transfers in hospitals.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0067-2015·2014-10-22

    Primus Medical Recalls AC Powered Adjustable Bed Frames

    Primus Medical LLC is recalling 1,726 AC powered adjustable bed frames used in nursing facilities because the head deck actuator bracket may separate from the frame.

    Product
    AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide