Philips recalls Allura Xper FD10C X-ray systems with system code 722001 due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair to ensure safe operation.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips is recalling Allura Xper FD10C X-ray systems with system code 722001 because the wired foot switch may not start X-ray imaging properly. This could lead to incomplete scans or failed procedures if the system doesn't respond as expected.
The X-ray imaging system may not start or may start intermittently when using the wired foot switch. This could cause incomplete scans or failed procedures if the system doesn't respond as expected during medical imaging.
Healthcare facilities using Philips Allura Xper FD10C X-ray systems with system code 722001 are likely affected. Medical staff and patients using these systems may be at risk of incomplete imaging procedures.
Check for system code 722001 on the device. The system serial number starts with 19,249,21,18661014,77,82,195,216,337,37,258,283,15,256,305.
Verify the system code is 722001 to confirm if your device is affected.
The recall indicates potential issues with X-ray imaging starting, but the hazard is not described as causing serious injury. The risk is low and related to incomplete procedures.
Check for system code 722001 on the device. The system serial number starts with 19,249,21,18661014,77,82,195,216,337,37,258,283,15,256,305.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1659-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1659-2026 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.
