Philips recalls ProxiDiagnost N90 Radiography and Fluoroscopy systems with potential for ceiling-mounted units to fail and fall. Affected models include specific serial numbers and UDI codes.
Potential for units suspended on the ceiling to fail and fall.
Philips is recalling ProxiDiagnost N90 Radiography and Fluoroscopy systems that may fail when suspended on the ceiling, causing them to fall. This poses a risk of injury if the unit falls on people or objects below.
The recalled systems are designed to be suspended on ceilings. If the mounting fails, the unit could fall and cause injury to people or damage to objects below. This risk is present in normal use conditions.
Healthcare facilities and medical professionals using the ProxiDiagnost N90 systems are most at risk. The recall affects specific models with serial numbers and UDI codes listed in the notice.
Check if your system has the model numbers 706100 or 706110 and the listed serial numbers or UDI codes. The recall covers specific units with the serial numbers provided in the notice.
Verify your system's model number and serial number against the list of affected units provided in the recall notice.
Reach out to Philips customer support for assistance with the recall process and to confirm if your unit is affected.
Philips recalls these systems because they may fail when suspended on the ceiling, potentially causing them to fall and pose a risk of injury.
Check your system's model number (706100 or 706110) and serial number against the list of affected units provided in the recall notice.
Contact Philips customer support to confirm if your unit is affected and follow their instructions for the recall process.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0280-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0280-2024 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.
