PHILIPS recalls ProxiDiagnost N9: After Lock-in command, x-ray settings may adjust if collimator shutter moves. No remedy stated in official notice.
After the user selects the Lock-in command, the kV and mA values are not locked immediately and can adjust if the collimator shutter position is changed directly after the Lock-in command.
PHILIPS is recalling its ProxiDiagnost N90 x-ray system because settings can change after a lock command if the collimator shutter is moved. This could lead to inconsistent x-ray images or potential safety issues during medical procedures.
After the user selects the Lock-in command, the kV and mA settings may adjust if the collimator shutter is moved immediately afterward. This could cause inconsistent x-ray images or unintended exposure during medical procedures.
Healthcare facilities using the ProxiDiagnost N90 x-ray system are likely affected. Medical staff performing x-ray procedures with this device are at risk of inconsistent imaging or potential safety issues.
The ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system is affected. No specific model numbers or dates are provided in the recall notice.
Verify if the device has the Lock-in command feature that may adjust settings after collimator shutter movement.
The official recall notice does not state any remedy or fix for this issue.
The ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system is affected, but no specific model numbers or dates are provided in the recall notice.
The recall indicates a potential for inconsistent x-ray images or unintended exposure, but no specific safety risks are described in the official notice.
We’ve drafted a message you can send PHILIPS HOME HEALTHCARE SOLUTION to request your refund or repair — edit it as you like.
Subject: Recall Z-0727-2021 — PHILIPS HOME HEALTHCARE SOLUTION PHILIPS HOME HEALTHCARE SOLUTION Hello, I own a PHILIPS HOME HEALTHCARE SOLUTION that is covered by recall Z-0727-2021 from PHILIPS HOME HEALTHCARE SOLUTION. 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.
