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.

426–450 of 681

  • HighFDA (Devices)·Z-0655-2016·2016-01-20

    Skytron Ergon 2 Monitor Brackets Recalled Due to Hardware Failure Risk

    Skytron is recalling 286 Ergon 2 monitor brackets because hardware may fail, causing displays to fall and potentially injure patients or providers.

    Product
    Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment penda
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0644-2016·2016-01-20

    CompView NuCARTGN Medical Display Recall Due to Spring Arm Detachment Risk

    CompView Medical is recalling 10 NuCARTGN mobile display units because the spring arm may detach if the securing ring was not installed correctly.

    Product
    Model NuCARTGN. The NuCART is a mobile display and image management platform used in Minimally Invasive Surgery (MIS) environments to facilitate the routing and ergonomic display of video signals from source devices to flat-panel monitors. It is tailored for use with an OEC C-a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V014000·2016-01-15

    Supreme Recalls Shuttle Buses Due to Wheelchair Lift Bearing Defect

    Supreme is recalling 2008-2014 shuttle buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.

    Product
    STARTRANS — STARTRANS CANDIDATE, SENTINEL BUS, AZURE HYBRID, PRESIDENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V009000·2016-01-13

    Turtle Top Recalls Wheelchair Lifts Due to Bearing Failure Risk

    Turtle Top is recalling specific wheelchair lifts installed in Odyssey and Terra Transport vehicles because pivot holes may allow bearings to move, risking platform failure.

    Product
    TURTLE TOP — TURTLE TOP ODYSSEY XL, ODYSSEY LT, ODYSSEY, TERRA TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0563-2016·2016-01-06

    Trumpf Ceiling Mounted Surgical Light Systems Recalled for Falling Hazard

    Trumpf Medical Systems is recalling 20,713 ceiling-mounted surgical light systems because the spring arm can detach, causing the light head to fall.

    Product
    Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V001000·2016-01-04

    AEV Ambulance Wheelchair Van Recall for Lift Bearing Defect

    Halcore is recalling 2006-2013 AEV Ambulance Wheelchair Vans because wheelchair lift bearings may move, causing the platform to fall and injure operators.

    Product
    AEV — AEV AMBULANCE WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V870000·2015-12-23

    Navistar Recalls IC Bus Transit Models Due to Wheelchair Lift Defect

    Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.

    Product
    IC BUS — IC BUS CE, FECB, FE, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V868000·2015-12-22

    Navistar Recalls School Buses with Defective Wheelchair Lifts

    Navistar is recalling certain 2007-2015 IC school buses equipped with specific Ricon wheelchair lifts. The lifts may have oversized pivot holes that allow bearings to shift, risking platform failure.

    Product
    IC BUS — IC BUS CASB, FE, RE, ICCB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16059·2015-12-16

    Skip Hop Recalls Crib Mobiles Due to Injury Hazard

    Skip Hop is recalling Moonlight & Melodies projection crib mobiles because the strap attaching the product to the crib rail can break, posing an injury hazard if the product falls on an infant.

    Product
    Skip Hop crib mobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16715·2015-12-15

    Lithonia Lighting Recalls JHBL LED Fixtures Due to Falling Risk

    Lithonia Lighting is recalling JHBL LED fixtures because the mounting hub can break, causing the fixture to fall. No injuries have been reported.

    Product
    JHBL LED Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0351-2016·2015-12-09

    Philips Allura Xper Cardio Systems Recalled for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling 16 Allura Xper cardio systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper cardio systems Model : 722123 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and throm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0354-2016·2015-12-09

    Philips Xper Vascular System Monitor Ceiling Suspension Recall

    Philips Medical Systems is recalling 22 Allura Xper vascular systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0349-2016·2015-12-09

    Philips INTEGRIS Vascular System Recall for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling three INTEGRIS vascular systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0353-2016·2015-12-09

    Philips Xper Cardio Systems Recalled for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling 14 Allura Xper Cardio systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0352-2016·2015-12-09

    Philips Xper Vascular System Recall for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling 10 Xper vascular systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper vascular system Model : 722124 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and thr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0348-2016·2015-12-09

    Philips INTEGRIS Cardio System Ceiling Suspension Recall

    Philips is recalling eight INTEGRIS cardio systems because the ceiling suspension system may fall.

    Product
    Philips Healthcare INTEGRIS cardio system Model : 722121 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0365-2016·2015-12-09

    Philips EasyDiagnost Patient Support Material Recalled for Footplate Safety Hazard

    Philips Medical Systems is recalling patient support materials for the EasyDiagnost device because the footplate hook may fail, causing the footplate to fall or swing and potentially injure patients or operators.

    Product
    Patient Support Material Number: 9890 010 87431, used with:EasyDiagnost ; Model: 706050
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·15V827000·2015-12-09

    Ameritrans Recalls Wheelchair Lifts with Potential Bearing Failure

    Ameritrans is recalling 2012-2014 buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.

    Product
    AMERITRANS — AMERITRANS CTV, 245, 395, 225
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0364-2016·2015-12-09

    Philips BuckyDiagnost Patient Support Material Recall for Footplate Safety

    Philips Medical Systems is recalling BuckyDiagnost patient support materials because the footplate hook may fail, causing the plate to fall or swing and injure patients or operators.

    Product
    Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0350-2016·2015-12-09

    Philips Allura X-Ray System Ceiling Suspension Recall

    Philips Medical Systems is recalling INTEGRIS H5000F/Allura 9F X-ray systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0346-2016·2015-12-09

    Philips Allura Xper Series Recall Due to Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling nine Allura Xper Series units because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper FD10/10 Allura Xper FD20 Allura Xper FD21 Allura Xper FD22 Allura Xper FD23 Allura Xper FD24 Allura Xper FD25 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0347-2016·2015-12-09

    Philips Allura BiPlane Ceiling Suspension System Recall for Fall Risk

    Philips Medical Systems is recalling five Allura BiPlane X-ray systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20 BIPLANE R7.6 722013 Allura Xper FD20 BIPLANE R7.7 722013 Allura Xper FD20 BIPLANE R7.8 722013 Allura Xper FD20 BIPLANE R7.9 722013 Allura Xper FD20 BIPLANE R7.10 Product Usage: The Allur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V779000·2015-11-20

    Ford E-Series Vans Recalled for Wheelchair Lift Bearing Defect

    New England Wheels is recalling 2006-2014 Ford E-250 and E-350 vans with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure the operator.

    Product
    FORD — FORD E-250, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V773000·2015-11-19

    Coach and Equipment Recalls Transit Buses with Defective Wheelchair Lifts

    Coach and Equipment is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts. The lifts may have pivot holes that allow bearings to move, risking platform failure.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT ALLEY CAT, METRO LITE, PEGASUS, PHOENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide