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.

576–600 of 681

  • HighNHTSA·13E036000·2013-07-05

    Thermo King Recalls Precedent S-600 Refrigeration Units Due to Bracket Defect

    Thermo King is recalling Precedent S-600 transportation refrigeration units manufactured in April and May 2013 because the lifting bracket may break, posing a risk of injury if the unit falls.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·13225·2013-06-25

    Bel Air Lighting Recalls Chandeliers Due to Falling Hazard

    Bel Air Lighting is recalling about 20,500 nine-light chandeliers because the mounting loop can break, causing the fixture to fall and pose an impact injury hazard.

    Product
    Portfolio and Transglobe nine-light chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13222·2013-06-20

    Kichler Aztec Chandeliers Recalled for Falling Hazard

    Kichler Lighting is recalling Aztec chandeliers sold at Lowe's because the fixture loop can fail, causing the light to fall from the ceiling.

    Product
    Aztec Light Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2013·2013-03-20

    GE Healthcare Recalls Cardiovascular X-ray Systems Due to Locking Nut Issue

    GE Healthcare is recalling specific cardiovascular X-ray imaging systems because a locking nut on the overhead video monitor suspension might loosen.

    Product
    GE Healthcare Advantx, Innova2000, Innova3100, Innova4100, Innova2100IQ, Innova3100IQ, and Innova4100IQ equipped with Video Monitor Suspension Cardiovascular X-ray imaging systems. Model numbers 2236709, 2353620 ,2223039-2, and 2270677-2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0926-2013·2013-03-20

    Medtronic O-arm Imaging System Recalled for Braking System Failure

    Medtronic is recalling 463 O-arm Imaging Systems worldwide due to a potential failure of the braking system controlling vertical gantry movement.

    Product
    Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic x-ray system, mobile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13E008000·2013-02-15

    Yakima SpareTime Bike Rack Recall Due to Mounting Bolt Failure

    Yakima is recalling SpareTime two-bike rack systems because mounting bolts may break, causing the rack to fall and create a road hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0657-2013·2013-01-16

    Stryker Recalls Surgical Light Spring Arms Due to Potential Separation Risk

    Stryker is recalling specific surgical light spring arms because a circlip may not engage fully, causing the arm to fall. No serious injuries have been reported.

    Product
    (l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring Arm Circlip is part of the Stryker Spring Arm used in multiple configurations as a component of the (1)Visum Halogen Surgical Light, (2)Visum LED Surgical Ligh
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0468-2013·2012-12-12

    Invivo Expression MRI Patient Monitoring System Recalled for Detached Caster Risk

    Invivo Corporation is recalling the Expression MRI Patient Monitoring System because a caster may detach during transport, causing the cart to fall.

    Product
    Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended for use by healthcare professionals to monitor vital signs for patients undergoing MRI procedures. The Patient Monitoring System also provides signals for sync
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0466-2013·2012-12-12

    Philips and Neusoft Recall CT Scanners Due to Detaching Patient Table

    Philips and Neusoft are recalling 45 CT scanners because the patient table top can detach from the carrier, posing a risk of injury.

    Product
    NeuViz 16 Multi-Sliced CT Scanner System, part number 989605858501. NeuViz Dual series CT Scanner System, part number 989605651321 The NeuViz 16 CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and det
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13050·2012-11-28

    G-U Hardware Recalls Window Fittings Due to Injury Hazard

    G-U Hardware is recalling approximately 5,000 window fittings because they can break, causing windows to fall and posing an injury hazard.

    Product
    Window Fittings: Tilt-turn Stay Arms and Side-hung Sash Hinges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0077-2013·2012-10-24

    Trumpf Medical Systems Recalls Helion and Xenion Surgical Lights

    Trumpf Medical Systems is recalling 275 Helion and Xenion surgical lights due to reported fractures of the front joint of the spring arm.

    Product
    Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2494-2012·2012-10-10

    Philips Digital Diagnost Patient Carriage Footplate Recall

    Philips is recalling Digital Diagnost patient carriages because the footplate hook may fail, causing the footplate to fall on patients or operators.

    Product
    Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2465-2012·2012-10-03

    Philips Digital Diagnost Mobile Detector Holder Recall for Insecure Fit

    Philips is recalling 93 Mobile Detector Holders because the Wireless Portable Detector may not be fixed securely and could fall down.

    Product
    Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System codes: 712020, 712022, 712025 This system is used for making X-ray exposures for diagnostics.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13002·2012-10-02

    Haier Recalls 42-inch LED TVs Due to Stand Neck Breakage Risk

    Haier America is recalling 42-inch LED TVs because the stand's neck support can break, causing the TV to tip over. No injuries have been reported.

    Product
    Haier America Trading 42-inch LED Televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2303-2012·2012-09-05

    Philips SureSigns VSi and VS2+ Patient Monitors Recalled for Mounting Defect

    Philips is recalling SureSigns VSi and VS2+ patient monitors because they may not be properly secured to wall mounts and could fall.

    Product
    Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279. The SureSigns VS2+ vital signs monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·12261·2012-08-29

    Cooper Lighting Recalls Shower Light Trim Due to Falling Hazard

    Cooper Lighting is recalling shower light trims because the trim and glass lens can fall from the ceiling, posing impact and laceration hazards.

    Product
    Shower light trim
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2207-2012·2012-08-22

    Philips Essenta DR X-Ray System Recalled Due to Potential C-Arm Fall

    Philips Healthcare Inc. is recalling seven Essenta DR X-ray systems because the C-arm may fall. The recall covers units distributed in the US and several international countries.

    Product
    Philips Essenta DR, X-Ray System, Diagnostic, general-purpose Model: 712070. The Essenta DR is a multifunctional stationary X-ray Intended Use From Labeling): system, in which the swivel arm rotation, the vertical movement of the swivel arm and the SID adjustment are motorize
    Category
    Medical Device
    Distribution
    3 states
  • HighCPSC·12249·2012-08-16

    Emerson Corsair Ceiling Fans Recalled Due to Falling Hazard

    Emerson is recalling Corsair ceiling fans because the hanger bracket can spread apart, causing the fan to fall from the ceiling.

    Product
    Emerson Corsair Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V342000·2012-07-19

    Collins Recalls 2012 School Buses Due to Electrical Panel Cover Defect

    Collins Bus Corporation is recalling 196 model year 2012 school and activity buses because the electrical panel cover may not be secured, posing a risk of falling and distracting the driver.

    Product
    CORBEIL — CORBEIL, COLLINS, MID-BUS DH, DE, SL, SH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12194·2012-06-07

    Bowflex SelectTech 1090 Dumbbells Recalled for Injury Hazard

    Nautilus is recalling Bowflex SelectTech 1090 Dumbbells because the weight selector dial can fail, causing weight plates to fall and injure users.

    Product
    Bowflex® SelectTech® 1090 Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12185·2012-05-23

    Cooper Lighting Recalls Commercial Reflector Assemblies Due to Falling Hazard

    Cooper Lighting is recalling about 21,000 commercial reflector assemblies because they can fall from fixtures, posing an injury risk. No injuries have been reported.

    Product
    Portfolio 7-inch reflector assembly with glass lens
    Category
    Consumer Product
    Distribution
    Distributed nationwide