FDAMarch 17, 2023device

Spectral CT 7500 Computed Tomography X-Ray System, Model Number 728333

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operators foot. If foot or leg entrapment occurs while pressing Unload Pedal, the risk to operators may include: pain, muscle or ligament sprain, abrasion, laceration, contusion, fracture, loss of function, and joint dislocation.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838101111

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Spectral CT 7500 Computed Tomography X-Ray System, Model Number 728333 — Recall Details · AllClear