Philips recalls BrightView SPECT SPECT scanners with model 882480 that may cause uncommanded handcontroller movements. Affected units have specific serial numbers listed in the recall notice.
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Philips is recalling BrightView SPECT SPECT scanners with model number 882480 due to a handcontroller that may move unexpectedly after button release. This could cause unintended motion during medical procedures.
The handcontroller may move unexpectedly either on its own or after the buttons are released, potentially causing unintended motion during medical procedures. This could lead to errors in imaging or patient safety issues.
Medical professionals using the BrightView SPECT SPECT scanners with model number 882480 and specific serial numbers listed in the recall notice are most at risk. Patients using these scanners may also be affected during procedures.
Check if your BrightView SPECT SPECT scanner has model number 882480 and one of the specific serial numbers listed in the recall notice. The serial numbers are provided in the official recall document.
Verify your BrightView SPECT SPECT scanner has model number 882480 and one of the listed serial numbers in the recall notice.
The handcontroller may move unexpectedly after button release, potentially causing unintended motion during medical procedures. This could lead to errors in imaging or patient safety issues.
Check if your BrightView SPECT SPECT scanner has model number 882480 and one of the specific serial numbers listed in the recall notice.
The recall notice does not specify a remedy, so you should check the official recall document for further instructions.
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-2009-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2009-2019 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.
