Philips recalls Azurion 7 M20 X-ray systems with specific system codes (722079, 722224, 722234, 722282) for potential failure to initiate X-ray imaging when using the wired foot switch.
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 certain Azurion 7 M20 X-ray imaging systems that may not start or intermittently stop X-ray imaging when using the wired foot switch. This could lead to incomplete scans or failed imaging procedures.
The X-ray imaging may not start or could stop intermittently when using the wired foot switch, potentially causing incomplete scans or failed imaging procedures during medical procedures.
Medical facilities using the recalled Azurion 7 M20 X-ray systems with specific system codes (722079, 722224, 722234, 722282) in the U.S. are most at risk.
Check if your Azurion 7 M20 system has one of the following system codes: 722079, 722224, 722234, or 722282 (sold only in the U.S.).
Identify your system code by checking the system serial numbers listed in the recall notice.
The Philips Azurion 7 M20 X-ray imaging system.
System codes 722079, 722224, 722234, and 722282 (sold only in the U.S.).
Check if your system has one of the system codes listed: 722079, 722224, 722234, or 722282.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1678-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1678-2026 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.
