Philips recalls Forte Gamma Camera Systems due to risk of detector falling unimpeded. Affected models include system codes 882290 and 882:1. No remedy specified in recall notice.
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 is recalling Forte Gamma Camera Systems because a detector component could fall vertically without obstruction, potentially causing damage. This recall affects medical imaging systems used in hospitals and clinics. The hazard is serious but does not involve immediate injury risk in normal use. No specific action is required per the recall notice.
The detector component in the camera system could fall vertically without obstruction to the end stops of its travel limit. This mechanical failure might cause the detector to impact the system frame or other components, potentially leading to system damage or malfunction during medical imaging procedures.
Medical facilities using Philips Forte Gamma Camera Systems with system codes 882290 or 882291 are most at risk. Hospital staff and medical personnel who operate these systems may be affected.
Check for system codes 882290 or 882291 on the Forte Gamma Camera System. These models were sold to medical facilities for imaging purposes.
Identify the system code on your Forte Gamma Camera System to determine if it is affected.
The recall notice does not specify a remedy or fix for this issue.
The recall notice does not provide specific action steps for affected systems.
Check for system codes 882290 or 882291 on the Forte Gamma Camera System.
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-0214-2020 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0214-2020 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.
