The Recall Desk

Hazard

Falling Object recalls

684 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
684
Critical
7
Severe
140
Most recent
2026-10-22

Of the 684 falling object recalls we have scored against our rubric, 7 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 140 (20%) 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 falling object 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.

76–100 of 684

  • HighNHTSA·21V757000·2021-09-28

    Rosenbauer Recalls Fire Trucks Due to Improperly Crimped Lifting Cables

    Rosenbauer America is recalling specific 2020-2022 fire trucks because improperly crimped lifting cables may detach, causing the generator set to fall and increasing injury risk.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL HV507, PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E075000·2021-08-17

    Cummins Recalls Generator Sets Due to Improperly Crimped Lifting Cables

    Cummins is recalling specific generator sets because lifting cables may be improperly crimped. This defect could cause the equipment to fall during lifting, increasing the risk of injury.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1268-2021·2021-03-24

    Carestream Dental CS 3600 Tips Recalled for Detachment Risk

    Carestream Dental is recalling CS 3600 Single Use Normal Tips because the mirror may become detached and fall from the unit.

    Product
    Carestream Dental CS 3600 Single Use Normal Tips, Catalog Number 5941216 - Product Usage: used to record the topographic characteristics of teeth or dental impressions in three dimensions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V130000·2021-03-02

    Ferrara Recalls 2009-2020 Aerial Vehicles Due to Trolley Defect

    Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.

    Product
    FERRARA — FERRARA AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2021·2021-02-17

    GE Healthcare Precision 600FP Monitor Suspension Recall

    GE Healthcare is recalling 113 Precision 600FP systems due to a potential monitor suspension defect that could cause injury.

    Product
    GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use by a qualified/trained doctor or technologist on both adult and pediatric subjects taking diagnostic radiographic and fluoroscopic exposures of the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2021·2021-02-10

    Philips EPIQ Ultrasound Systems Recalled for Control Panel Failure Risk

    Philips is recalling 12,080 EPIQ Diagnostic Ultrasound Systems because the control panel arm assembly may break off if subjected to undue force.

    Product
    Philips EPIQ Diagnostic Ultrasound System, Models EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx & EPIQ CVxi - Product Usage: the systems can assist the interventionist and surgeon with image guidance during treatment of cardiovascular disease in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0806-2021·2021-01-20

    Siemens Uroskop Omnia Max X-ray System Recalled for Support Arm Risk

    Siemens is recalling 281 Uroskop Omnia Max X-ray systems because the monitor support arm may become dislodged after intense, long-term use.

    Product
    Uroskop Omnia Max, Model no. 10762473 - Product Usage: a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20E094000·2020-12-28

    Summit Racing 6-Ton Jack Stands Recalled Due to Ratchet Bar Failure Risk

    Autosales Inc. is recalling Summit Racing 6-Ton Jack Stands because the ratchet bar may fail, allowing the vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.

    Product
    EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E093000·2020-12-23

    Autosales Recalls Summit Racing 3-Ton Jack Stands Due to Ratchet Bar Failure

    Autosales is recalling Summit Racing 3-Ton Jack Stands because the ratchet bar may fail, allowing a vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.

    Product
    EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V804000·2020-12-21

    Thor Motor Coach Recalls 2018-2019 Hurricane and Windsport Motorhomes

    Thor Motor Coach is recalling 2018-2019 Hurricane and Windsport motorhomes because overhead cabinets may detach and fall on occupants.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21034·2020-11-25

    RH Recalls Wine Barrel Chandeliers Due to Falling Hardware Hazard

    RH is recalling approximately 7,800 wine barrel chandeliers because hanging hardware can break, causing the fixture to fall. No injuries have been reported.

    Product
    Wine Barrel Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E074000·2020-10-06

    Lippert Components Recalls Electric Motors in Power Bedlift Systems

    Lippert Components is recalling electric motors in Power Bedlift systems because internal gear failure may cause the bed to extend unexpectedly, increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E073000·2020-10-02

    Dick's Sporting Goods Recalls Field & Stream Kayak Cradles

    Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20183·2020-09-16

    RH Recalls Industrial Three-Panel Mirrors Due to Injury Hazard

    RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.

    Product
    Industrial Three-Panel Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20774·2020-09-03

    StoreYourBoard Recalls Hi-Lift Storage Hoists Due to Strap Breakage Hazard

    StoreYourBoard.com is recalling Hi-Lift Storage Hoists because green polypropylene straps can break, causing stored items to fall and potentially injure passersby.

    Product
    Hi-Lift Storage Hoist Classic and Pro models sold with green polypropylene straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2330-2020·2020-06-17

    Medtronic Mazor X Surgical System Positioner Recalled for Detachment Risk

    Medtronic is recalling 177 Mazor X Surgical System Positioner Type II units because they may unexpectedly detach from the operating table, posing a risk of blunt injury to patients.

    Product
    Mazor X Surgical System Positioner Type II, REF: ASM0214-02
    Category
    Medical Device
    Distribution
    28 states
  • HighCPSC·20134·2020-06-10

    Ushio America Recalls Indiglow LED T8 Lamps Due to Overheating Hazard

    Ushio America is recalling Indiglow LED T8 lamps because they can overheat and fall, posing an injury risk. Consumers should stop using them and contact the company for a refund or replacement.

    Product
    Indiglow LED T8 Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1806-2020·2020-05-06

    Philips TraumaDiagnost X-Ray System Recalled Due to Potential Shaft Failure

    Philips North America is recalling 346 TraumaDiagnost X-Ray systems because a shaft may break due to material fatigue, causing the arm to fall and potentially injure patients or staff.

    Product
    Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
    Category
    Medical Device
    Distribution
    Distributed nationwide