Philips recalls Spectral CT 7500 X-Ray Systems (model 728333) due to risk of foot entrapment during operation, potentially causing injury. Affected units have specific serial numbers listed in the recall notice.
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.
Philips is recalling its Spectral CT 7500 Computed Tomography X-Ray Systems (model 728333) because pressing the Unload Pedal can cause foot entrapment, leading to injuries like fractures or dislocations. This risk affects medical professionals who use the device daily.
Pressing the Unload Pedal during operation can trap the operator's foot, potentially causing pain, sprains, lacerations, fractures, or joint dislocations. This hazard occurs when the foot switch is used incorrectly or without proper awareness of the mechanism.
Healthcare professionals who operate the Spectral CT 7500 X-Ray System are most at risk. The recall applies to specific units with serial numbers listed in the official notice.
Check if your Spectral CT 7500 X-Ray System has the model number 728333 and serial numbers listed in the official recall notice (e.g., 10058, 10074, 10080, etc.).
Inspect the Unload Pedal for signs of improper operation that could cause foot entrapment.
The affected model number is 728333 for Philips Spectral CT 7500 Computed Tomography X-Ray Systems.
Check if your unit has the model number 728333 and serial numbers listed in the official recall notice (e.g., 10058, 10074, 10080, etc.).
Injuries could include pain, muscle or ligament sprains, abrasions, lacerations, contusions, fractures, loss of function, or joint dislocations.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1584-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-1584-2023 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
