Philips recalls Forte Gamma Camera Systems due to potential detector falling unimpeded, which could cause injury. Affected units may need repair or replacement.
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 could fall vertically without obstruction, posing a risk of injury. This is a safety issue for medical facilities using the equipment.
The detector in the camera system could fall unimpeded to the end stops of its travel limit. This movement might cause injury to personnel if the detector strikes someone or equipment during use.
Medical facilities using Philips Forte Gamma Camera Systems are likely affected. Staff handling the equipment are at higher risk due to the potential for injury during operation.
The affected units are Philips Forte Gamma Camera Systems with System Code 882: All systems are included in this recall. This recall applies to all units sold by Philips Medical Systems.
Verify the system code on your camera to confirm if it is affected (System Code 882020).
Yes, all Forte Gamma Camera Systems with System Code 882020 are included in this recall.
The recall does not specify a remedy, so contact Philips Medical Systems for further instructions.
The recall states that the detector could fall unimpeded, which might cause injury, but the exact risk level is not specified.
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-0213-2020 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0213-2020 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.
