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.

251–275 of 681

HighFDA (Devices)·Z-3236-2018·2018-10-03
Philips Allura Xper F020 Biplane DR Table Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F020 Biplane DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper F020 Biplane DR Table, System Code 722020 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3214-2018·2018-10-03
Philips INTEGRIS Allura 9 Biplane Recall for Monitor Suspension Defect
Philips is recalling INTEGRIS Allura 9 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3216-2018·2018-10-03
Philips INTEGRIS Allura Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3229-2018·2018-10-03
Philips FlexVision Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling FlexVision Monitor Ceiling Suspensions because the monitor may detach from the actuator rotor shaft, posing a risk of injury to patients, users, and bystanders.
Product
AIIuraXperFDlO, System Code 722010 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3213-2018·2018-10-03
Philips INTEGRIS Allura 9 Monitor Ceiling Suspension Recall
Philips is recalling INTEGRIS Allura 9 systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.
Product
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3231-2018·2018-10-03
Philips AIIura Xper F010 DR Table Recall for Monitor Detachment Risk
Philips is recalling AIIura Xper F010 DR Tables because the ceiling monitor suspension may detach, posing a risk of injury to patients and staff.
Product
AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3225-2018·2018-10-03
Philips Allura Xper FD1O C Ceiling Monitor Recall for Detachment Risk
Philips is recalling 5,115 Allura Xper FD1O C systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD1O C, System Code 722001 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3217-2018·2018-10-03
Philips INTEGRIS Allura 15-12 Biplane Monitor Suspension Recall
Philips is recalling INTEGRIS Allura 15-12 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 15-12 (biplane), System Code 722044 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3224-2018·2018-10-03
Philips Allura Xper FD2O Biplane Recall for Monitor Suspension Detachment Risk
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3223-2018·2018-10-03
Philips Allura Xper FD2O Biplane Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.
Product
Allura Xper FD2O Biplane, System Code 722013 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3238-2018·2018-10-03
Philips Medical Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach from the actuator, posing a risk of injury to patients and users.
Product
Cesar-DMCP-Visub(HM2000/3000), System Code 72239 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3215-2018·2018-10-03
Philips INTEGRIS CV Ceiling Monitor Suspension Recall for Detachment Risk
Philips is recalling INTEGRIS CV systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS CV, System Code 722030 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3221-2018·2018-10-03
Philips Allura Xper FD2O Ceiling Monitor Suspension Recall
Philips is recalling 5,115 Allura Xper FD2O systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3226-2018·2018-10-03
Philips AlIura Xper F010 F Monitor Ceiling Suspension Recall
Philips is recalling AlIura Xper F010 F systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
AlIura Xper F010 F, System Code 722002 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3235-2018·2018-10-03
Philips Allura Xper F010/10 DRTable Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F010/10 DRTables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper F010/10 DRTable, System Code 722019 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3237-2018·2018-10-03
Philips Medical Monitor Ceiling Suspension Recall Due to Detachment Risk
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach from the actuator rotor shaft and fall, posing a risk of injury to patients, users, and bystanders.
Product
Poly C- DMCP-Visub(H3000), System Code 72238 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3219-2018·2018-10-03
Philips INTEGRIS Allura 9 F FDXD Monitor Suspension Recall
Philips is recalling INTEGRIS Allura 9 F FDXD systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 9 F FDXD, System Code 722497 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3228-2018·2018-10-03
Philips AlluraXperFOlO/lO Ceiling Monitor Suspension Recall
Philips is recalling 5,115 AlluraXperFOlO/lO systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients or users.
Product
AlluraXperFOlO/lO, System Code 722005 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3218-2018·2018-10-03
Philips INTEGRIS SUITE Ceiling Monitor Suspension Recall
Philips is recalling INTEGRIS SUITE systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients or users.
Product
INTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3220-2018·2018-10-03
Philips NTEGRIS Allura 9 0 FDXD Ceiling Monitor Recall
Philips is recalling NTEGRIS Allura 9 0 FDXD systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
NTEGRIS Allura 9 0 FDXD, System Code 722498 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3234-2018·2018-10-03
Philips Allura Xper F020 DR Table Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F020 DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper F020 DR Table, System Code 722015 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2961-2018·2018-09-12
Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure
Bayer Medical Care is recalling one Overhead Counterpoise System unit due to potential overtightening of bolts that could compromise structural integrity.
Product
Overhead Counterpoise Systems (OCS) OCS CONF an accessory device for use with Bayer injector systems as a support for an injector head. , SHORT CEIL MNT, STD HORZ ARM, Catalog # OCS 115AS, Material Number 59880288
Category
Medical Device
Distribution
3 states
SevereNHTSA·18V590000·2018-09-05
Fabform Recalls 2017-2018 Power Tilt Dump Trailers Due to Hinge Fracture Risk
Fabform is recalling 2017-2018 Power Tilt 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 POWER TILT DUMP TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2838-2018·2018-08-29
Siemens 3D V Ceiling Stand Recalled for Potential Rope Failure
Siemens is recalling 3D V ceiling stands because the primary load-bearing rope could break, causing the arm to drop and potentially seriously injuring patients or users.
Product
3D V, model. no. 7042042 7042059 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the detector and is moveable on a ceiling rail system in three axis. The tube and / or detector can be rotated above a horizontal and a vertical axle. The c
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2848-2018·2018-08-29
Philips DigitalDiagnost 2.x Upgrades Recalled Due to Footplate Safety Hazard
Philips is recalling DigitalDiagnost 2.x Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081
Category
Medical Device
Distribution
Distributed nationwide