Philips recalls certain CombiDiagnost R90 radiography systems that may fail and fall from ceiling mounts, posing a fall hazard. Affected units have specific serial numbers.
Potential for units suspended on the ceiling to fail and fall.
Philips is recalling certain CombiDiagnost R90 radiography and fluoroscopy systems that may fail and fall from ceiling mounts. This could cause injury if the unit falls on people or objects below.
The recalled units have a potential to fail and fall from ceiling mounts. If the unit falls, it could cause injury to people or damage to objects below, especially in medical environments where equipment is close to staff and patients.
Healthcare facilities using the recalled CombiDiagnost R90 systems are most at risk, as these units are typically installed in medical settings where they could fall onto people or equipment.
Check if your CombiDiagnost R90 system has a serial number listed in the provided list of affected units. The serial numbers start with SN or 10000000 and include specific patterns like SN17000014 or 10000020.
Look for the serial number on your CombiDiagnost R90 system to see if it matches the list of affected units provided in the recall notice.
The recall is for potential failure and falling of the CombiDiagnost R90 system from ceiling mounts, which could cause injury if it falls on people or objects below.
Check if your system's serial number matches the list of affected units provided in the recall notice, which includes specific patterns like SN17000014 or 10000020.
The recall does not specify a remedy, so contact Philips directly to determine next steps for affected units.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0271-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0271-2024 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.
