The Recall Desk

Hazard

Falling Object recalls

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

What the numbers show

Total
681
Critical
7
Severe
133
Most recent
2026-08-20

Of the 681 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 133 (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.

301–325 of 681

  • HighFDA (Devices)·Z-2858-2018·2018-08-29

    Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk

    Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.

    Product
    DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2853-2018·2018-08-29

    Philips DigitalDiagnost 4.1 Chest X-Ray Unit Recalled for Footplate Hazard

    Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2846-2018·2018-08-29

    Philips BuckyDiagnost Ceiling System Recalled for Footplate Safety Hazard

    Philips is recalling BuckyDiagnost Ceiling Systems because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.

    Product
    BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V565000·2018-08-27

    Fabform Recalls 2018 EPT Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2018 EPT dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V520000·2018-08-07

    Terex Recalls 2015-2018 Digger Derricks Due to Weld Defect

    Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.

    Product
    TEREX — TEREX C4000, GENERAL 80, C6000, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2555-2018·2018-08-01

    Leica M320 Microscope Systems Recalled for Gas Spring Bracket Failure

    Leica Microsystems is recalling 8,564 M320 Microscope Systems because screws holding the gas spring bracket may fail, causing the optics carrier to drop.

    Product
    Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419, 10448420, 10448485, 10448486 Product Usage: Intended use of this device is an optical instrument for magnifying and illuminating specimens. It can be applied for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2502-2018·2018-07-25

    Maquet VOLISTA StandOP Surgical Light Recall for Detachment Risk

    Maquet is recalling 151 VOLISTA StandOP surgical lights due to a potential light head detachment issue that could cause serious injury.

    Product
    VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF AIM STP; ARD568821911 VLT600SF AIM STP QL; ARD568821910 VLT600SF STP QL; ARD568811901 VLT600SF AIM STP Product Usage: The Maquet VOLISTA surgic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18E061000·2018-07-25

    Rock Run Recalls LP Bottle Ring Brackets for Propane Tank Safety

    Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V463000·2018-07-11

    Pierce Emergency Vehicles Recalled for Aerial Bracket Detachment Risk

    Pierce is recalling 2007-2017 emergency vehicles because an aerial device bracket may detach and fall, potentially striking a person below.

    Product
    PIERCE — PIERCE ARROW XT, ENFORCER, QUANTUM, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2248-2018·2018-06-27

    Siemens Biograph mCT Systems Recalled Due to Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 405 Biograph mCT systems because laser cover windows may fall off, posing a potential hazard.

    Product
    Biograph mCT Systems: (a) Biograph mCT S(64)-3R, Material Number 10248669 Product Usage: The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·18176·2018-06-12

    Uttermost Recalls Mirrors and Wall Decor Due to Falling Hazard

    Uttermost is recalling about 17,000 mirrors and wall decor items because the hanging hardware can break, causing items to fall and injure bystanders.

    Product
    Mirrors, art and wall decor
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1927-2018·2018-05-30

    Getinge Recalls ALM XTEN Surgical Lights Due to Broken Spring Arms

    Getinge is recalling 667 ALM XTEN Surgical Lights because spring arms may crack and break, causing light heads to separate.

    Product
    ALM XTEN Surgical Light intended to provide visible illumination for the surgical field or for the examination of the patient. Part Numbers: ARD567801093, ARD567801094
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1880-2018·2018-05-23

    Visaris Diagnostic X-Ray System Recalled for Tube Arm Suspension Failure

    Visaris DOO is recalling specific diagnostic X-ray systems due to a potential failure in the tube arm suspension that could cause the arm to descend uncontrollably.

    Product
    Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.2 The Vision systems are intended for use in all areas of diagnostic radiography imaging and specifically at secondary and tertiary levels of medical care. Powerful positioning capability makes this syste
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1882-2018·2018-05-23

    Visaris Diagnostic X-Ray System Recalled for Tube Arm Suspension Failure

    Visaris DOO is recalling 22 diagnostic X-ray systems worldwide due to a potential failure of the tube arm suspension that could cause an uncontrollable descent and injury.

    Product
    Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.4 The Vision systems are intended for use in all areas of diagnostic radiography imaging and specifically at secondary and tertiary levels of medical care. Powerful positioning capability makes this syste
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1881-2018·2018-05-23

    Visaris Diagnostic X-Ray Systems Recalled for Tube Arm Suspension Failure Risk

    Visaris DOO is recalling 22 diagnostic X-ray systems worldwide due to a potential failure of the tube arm suspension that could cause an uncontrollable descent and patient injury.

    Product
    Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.3 The Vision systems are intended for use in all areas of diagnostic radiography imaging and specifically at secondary and tertiary levels of medical care. Powerful positioning capability makes this system
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1642-2018·2018-05-16

    Maquet Cardiohelp Gas Bottle Holder Recalled for Potential Clamp Failure

    Maquet Cardiopulmonary Ag is recalling 14 units of the Cardiohelp Gas Bottle Holder HKH 8880 because the clamps may crack or break during strong vibrations.

    Product
    CARDIOHELP Gas Bottle Holder HKH 8880, Product Code/Part Number 70105.0901 Product Usage: The Cardiohelp Gas Bottle (or Cylinder) Holder HKH 8880 is an accessory for the CARDIOHELP System and required for inter-hospital patient transport in aircraft and road vehicles (mobile
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·18V292000·2018-05-03

    Jayco Jay Series Trailers Recalled for Roof Lift Mechanism Defect

    Jayco is recalling 2011 and 2013 Jay Series camping trailers because misuse of the manual roof lift override may damage the mechanism, causing the roof to fall unexpectedly.

    Product
    JAYCO — JAYCO JAY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V276000·2018-04-30

    Altec Heartland Boom-Mounted Saw Recall Due to Valve Adjustment Issue

    Altec is recalling 2017-2018 EC175, EC225, and EC655 Boom-Mounted Saw vehicles because a valve may allow tree trunks to slip or fall, increasing injury risk.

    Product
    ALTEC HEARTLAND — ALTEC HEARTLAND EC225 BOOM-MOUNTED SAW, EC655 BOOM-MOUNTED SAW, EC175 BOOM-MOUNTED SAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1379-2018·2018-04-25

    Getinge Washer-Disinfector Accessory Recall for Potential Cart Unloading Hazard

    Getinge is recalling 170 automated loading/unloading accessories for Washer-Disinfector 86 Series units due to a risk of disinfected goods falling to the floor.

    Product
    Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 86 Series UDI Info: 86 Series Washer Disinfector 07340153700246, 07340153700253, 07340153700260, 07340153700277 Getinge automated loading/unloading systems are intended to be used as an automatic conveyor/transpor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1380-2018·2018-04-25

    Getinge Washer-Disinfector Accessory Recall Due to Unloading Hazard

    Getinge is recalling 170 automated loading/unloading systems for Washer-Disinfector 88 Series units. The recall addresses a risk that disinfected goods may fall to the floor if the trolley is not docked.

    Product
    Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 88 Series UDI Info: 07340153700109, 07340153700116 Getinge automated loading/unloading systems are intended to be used as an automatic conveyor/transport system for unloading carriers (wash carts) from Getinge 86/
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1318-2018·2018-04-18

    Reliance Medical Products Recalls Refractor Suspension Arms Due to Missing Parts

    Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.

    Product
    Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a refractor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2018·2018-04-11

    Seiler Alpha Air 6 ENT Microscope Recalled for Tipping Hazard

    Seiler Instruments is recalling Alpha Air 6 ENT Microscopes because they may tip over if attachments are extended and the device is moved improperly.

    Product
    Alpha Air 6 ENT Microscope Microscope examination of the human ear, nose, and throat.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0717-2018·2018-03-07

    Philips Allura Xper FD X-ray Systems Recalled for Monitor Fall Hazard

    Philips is recalling 1,486 Allura Xper FD and ORT X-ray systems because extra monitors mounted on the ceiling suspension may disengage and fall.

    Product
    Allura Xper FD and and Xper FD ORT - Philips X-ray Systems Product Usage: The Allura Xper FD10 and Alllura Xper FD10/10 is intendd for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0595-2018·2018-02-21

    Hologic Panther Fusion Recalled Due to Falling Glass Panel Hazard

    Hologic is recalling 103 Panther Fusion instruments because the glass panel may separate from the monitor and fall, potentially striking an operator.

    Product
    Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 Product Usage: The Panther instrument is a fully automated sample-to-result instrument, eliminating the need for batch processing and automates all aspects of nucleic acid testing on a single, integrated platform. The Pa
    Category
    Medical Device
    Distribution
    0 states