Philips recalls Forte Gamma Camera Systems due to risk of detector falling unimpeded, potentially causing injury. Affected units have specific system codes and serial numbers.
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 that may have a detector that falls unimpeded, posing a risk of injury. This recall affects medical imaging equipment used in healthcare settings.
The detector in the camera system may fall vertically without obstruction to the end stops of its travel limit. This could cause injury if the detector impacts a person or object during use.
Healthcare facilities using Philips Forte Gamma Camera Systems are most at risk. Medical personnel and patients using these systems could be affected.
Check for system code 889456 and serial number 24 on the Forte Gamma Camera System. This recall applies to specific models sold for medical imaging.
Verify the system code (889:456) and serial number (24) on your Forte Gamma Camera System.
The detector may fall unimpeded to the end stops of its travel limit, potentially causing injury.
Check the system code (889456) and serial number (24) to confirm if your unit is affected.
The recall record does not specify a remedy or fix.
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-0216-2020 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0216-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
