Hazard
684 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
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
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.
Haier is recalling 55-inch LED televisions installed in fifth-wheel recreational vehicles because mounting brackets may separate, causing the TVs to fall.
IKEA is recalling HYBY and LOCK ceiling lamps because plastic clips can break, causing glass shades to fall and pose a laceration hazard.
Altec Industries is recalling 2015 Effer 440 and 470 Knuckle Boom Cranes because pedestal welds may crack, potentially causing the crane to fall and injure people.
CompView Medical is recalling 10 NuCARTGN mobile display units because the spring arm may detach if the securing ring was not installed correctly.
Skytron is recalling 286 Ergon 2 monitor brackets because hardware may fail, causing displays to fall and potentially injure patients or providers.
Supreme is recalling 2008-2014 shuttle buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.
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.
Trumpf Medical Systems is recalling 20,713 ceiling-mounted surgical light systems because the spring arm can detach, causing the light head to fall.
Halcore is recalling 2006-2013 AEV Ambulance Wheelchair Vans because wheelchair lift bearings may move, causing the platform to fall and injure operators.
Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.
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.
Casablanca is recalling about 30,000 ceiling fans because the motor and blades can fall off during reverse operation, posing an injury risk.
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.
Lithonia Lighting is recalling JHBL LED fixtures because the mounting hub can break, causing the fixture to fall. No injuries have been reported.
Philips Medical Systems is recalling 16 Allura Xper cardio systems because the monitor ceiling suspension system may fall.
Philips Medical Systems is recalling 22 Allura Xper vascular systems because the monitor ceiling suspension system may fall.
Philips Medical Systems is recalling 14 Allura Xper Cardio systems because the monitor ceiling suspension system may fall.
Philips Medical Systems is recalling three INTEGRIS vascular systems because the monitor ceiling suspension system may fall.
Ameritrans is recalling 2012-2014 buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
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.
Philips is recalling eight INTEGRIS cardio systems because the ceiling suspension system may fall.
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.
Philips Medical Systems is recalling 10 Xper vascular systems because the monitor ceiling suspension system may fall.
Philips Medical Systems is recalling INTEGRIS H5000F/Allura 9F X-ray systems because the monitor ceiling suspension system may fall.
Philips Medical Systems is recalling nine Allura Xper Series units because the monitor ceiling suspension system may fall.