Philips Medical Systems recalls Forte Gamma Camera Systems due to potential detector falling. Affected units may require repair or replacement to prevent injury during medical imaging.
An issue with the Detector for the Forte Family of cameras may result in either detector 1 or detector 2 falling unimpeded vertically to the end stops of its travel limit.
Philips recalls certain Forte Gamma Camera Systems that could have detectors falling and potentially causing injury. This is a safety issue for medical facilities using the equipment.
The detector in the camera system may fall vertically without obstruction to the end stops. This could cause injury to medical personnel or patients during imaging procedures if the camera malfunctions.
Medical facilities using the recalled Forte Gamma Camera Systems are most at risk. Patients and staff could be affected if the camera malfunctions during imaging procedures.
Check for the System Code 889471 and Serial Number 1 on the camera system. The recall applies to specific models used in medical imaging.
Verify the System Code and Serial Number on the camera system to confirm if it is affected.
The detector in the Forte Gamma Camera System may fall vertically without obstruction, potentially causing injury during medical imaging procedures.
Check the System Code and Serial Number to see if it is affected. If affected, contact Philips Medical Systems for further instructions.
The recall indicates a potential risk of injury if the detector falls, but the remedy is not specified in the record.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0217-2020 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0217-2020 from Philips Medical Systems. 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.
