Philips recalls certain Gemini TF Big Bore PET/CT monitors due to potential bracket detachment causing serious injury if the monitor falls while attached to cables.
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Philips is recalling specific Gemini TF Big Bore PET/CT monitors because the monitor bracket assembly may detach, causing the monitor to fall and potentially injure patients, operators, or others. This hazard occurs when the monitor is in use and attached to cables.
The monitor bracket assembly may wear without being noticed, leading to detachment from the suspension arm. If the monitor falls while still connected to cables, it could cause serious injury to people nearby.
Healthcare facilities using the recalled monitors are most at risk. Patients, medical staff, and anyone near the monitor during procedures could be injured if it falls.
The recalled product is the Philips Gemini TF Big Bore PET/CT monitor with model number 882476. This model was sold without a serial number or unique device identifier.
Immediately stop using the recalled monitor to prevent potential injury from falling.
No, this recall is for medical facilities using the monitor in clinical settings.
Check for model number 882476 on the monitor. This model was sold without a serial number or unique device identifier.
The recall does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1989-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-1989-2021 from Philips. 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.
