Philips recalls certain IQon Spectral CT monitors due to potential bracket detachment causing falls and serious injury to patients or staff. Affected models include specific serial numbers listed in the recall notice.
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 models of IQon Spectral CT monitors that may have a bracket assembly that wears down and detaches, risking the monitor falling and causing serious injury to patients, operators, or bystanders. Owners should stop using these models immediately.
The monitor bracket assembly can wear down over time and become detached from the suspension arm. If this happens, the monitor may fall while still attached to its cables, posing a serious injury risk to anyone nearby.
Healthcare facilities using the recalled IQon Spectral CT monitors are most at risk, as the monitor could fall while still connected to cables, potentially injuring patients, medical staff, or others nearby.
Check for the model number 728332 with specific serial numbers listed in the recall notice. The product is a ceiling-mounted CT monitor used in medical facilities.
Discontinue use of the recalled IQon Spectral CT monitor to prevent potential injury from falling.
The recall affects IQon Spectral CT monitors with model number 728332 and specific serial numbers listed in the notice.
Check if your monitor has model number 728332 and one of the specific serial numbers listed in the recall notice.
The recall does not provide a fix; the remedy is not stated in the notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1985-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-1985-2021 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.
