Philips recalls Azurion 7 M12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using wired foot switch. Affected units may require repair or replacement.
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 Azurion 7 M12 X-ray imaging systems with certain system codes because they may not start or intermittently stop X-ray imaging when using the wired foot switch. This could lead to incomplete scans or missed diagnoses.
The X-ray imaging may not start or could stop intermittently when using the wired foot switch. This could result in incomplete scans or missed diagnoses during medical procedures, potentially affecting patient care outcomes.
Healthcare facilities using Philips Azurion 7 M12 systems with system codes 722078, 722223, or 722233 are most at risk. Patients undergoing X-ray procedures may experience incomplete imaging if the system fails to initiate properly.
Check for system codes 722078, 722223, or 722233 on the device. These codes are part of the system's identification and can be found in the device's documentation or on the system's label.
Identify the system code on your device to confirm if it is affected (722078, 722223, or 722233).
Reach out to Philips for guidance on next steps, including potential repairs or replacements.
The affected system codes are 722078, 722223, and 722233.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
No, but you should check the system code and contact Philips 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-1677-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1677-2026 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.
