Philips recalls CT X-Ray System Model 72814 due to risk of foot entrapment when pressing the unload pedal. Affected units have specific serial numbers listed in the recall notice.
Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury
Philips is recalling its Incisive CT X-Ray System model 72814 because pressing the unload pedal can cause foot entrapment and injury. This hazard affects medical professionals who use the device daily, as improper operation could lead to serious foot injuries.
Pressing the unload pedal of the foot switch can trap the operator's foot, leading to injury. This happens during the normal operation of the device when the pedal is activated to perform the unload function. The risk is present in the device's design without requiring additional actions from the user.
Medical professionals using the Philips Incisive CT X-Ray System model 72814 are most at risk. The hazard occurs when the operator presses the unload pedal during normal use, potentially causing foot entrapment.
Check for the model number 72814 on the device. Affected units have specific serial numbers listed in the recall notice, including US and OUS serial numbers provided in the record.
Identify the model number on the device, which should be 72814 for affected units.
Reach out to Philips North America for assistance with the recall process.
The model number is 72814.
Check for the model number 72814 and specific serial numbers listed in the recall notice, including US and OUS serial numbers provided in the record.
Contact Philips North America for assistance with the recall process.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1585-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-1585-2023 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.
