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.
Milestone AV Technologies is recalling Sanus Simplicity SLF5 wall mounts because a nut can loosen, causing the TV to detach and pose an impact hazard.
Mobility Works is recalling 834 Ford E-Series vans modified with Ricon wheelchair lifts. The platform side plates may crack, causing the lift to fall and injure the operator.
Rejuvenation is recalling about 85 Haleigh Wire Dome Pendant lamps because the cord system can fail, causing the lamp to fall and pose a risk of injury.
GE Healthcare is recalling Precision 500D X-ray systems because missing screws may cause the overhead video monitor to detach from the tray assembly.
Trans Tech is recalling 188 school buses equipped with Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk to operators.
New England Wheels is recalling 2006-2014 Ford E-250 and E-350 vans with specific Ricon wheelchair lifts because the platform side plate may crack.
Diamond Coach is recalling 45 model year 2006-2011 PT and VIP buses because wheelchair lift platform side plates may crack, posing an injury risk.
Forest River is recalling 2006-2014 Glaval buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing a risk of injury.
Elkhart Coach is recalling 2006-2014 Ford E-350 and E-450 vans equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
National Van is recalling 2007-2014 Ford E-150 and E-250 vans equipped with specific Ricon wheelchair lifts. The platform side plates may crack, causing the lift to fall and injure the operator.
GE Healthcare is recalling 334 Discovery XR656P/N wall stand systems because nylon hooks supporting the detector may fail, causing the detector to fall.
Carestream Health is recalling 589 Kodak DirectView DR 7500 diagnostic x-ray systems because the x-ray tube assembly may detach from the overhead crane due to insufficiently tightened hardware.
Attwood is recalling kayak and watersports storage hangers because the length adjustment buckles may release unexpectedly, causing stored items to fall and injure people nearby.
Blue Bird is recalling certain 2007-2015 school buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.
Far East Brokers is recalling glass beverage dispenser sets sold at Publix because the metal stand can break, posing an injury hazard.
Stryker Communications is recalling SHAPE Arm monitor mounts because the mount may detach if a lock washer and screw are missing.
Stryker Communications is recalling 953 SHAPE Arm components because the monitor mount may detach if a lock washer and screw are missing.
Stryker Communications is recalling 953 SHAPE Arm brackets used in operating rooms because the monitor mount may detach if specific hardware is missing.
Stryker Communications is recalling SHAPE Arm Dual SH2 brackets because the monitor mount may detach if specific hardware is missing.
Stryker Communications is recalling 953 SHAPE Arm brackets because the monitor mount may detach if a lock washer and screw are missing.
GE Healthcare is recalling Revolution XR/d digital radiographic systems because a collimator installation error during maintenance could cause the device to fall and injure patients.
GE Healthcare is recalling Proteus XR/a and Revolution XR/d X-ray systems due to a collimator installation error that caused a serious patient injury.
Leica Microsystems is recalling 103 MSF-1 ceiling mounts because a broken drive screw caused the lift arm to fall approximately 60 cm.
Leica Microsystems is recalling 103 ceiling mounts for M500 N microscopes because a broken drive screw caused the lift arm to fall approximately 60 cm.
GE Healthcare is recalling Kenex ceiling suspended radiation shields and surgical lamps due to improper installation. A reported incident involved a shield falling from the ceiling.