Philips recalls Azurion 3 M15 X-ray systems with specific system codes due to 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 3 M15 X-ray systems because they may not start or intermittently stop X-ray imaging when using the wired foot switch. This could lead to incomplete medical imaging procedures.
The wired foot switch may fail to initiate X-ray imaging or cause intermittent imaging, which could result in incomplete medical imaging procedures. This might lead to inaccurate diagnoses or delayed treatment.
Healthcare facilities using the recalled Azurion 3 M15 X-ray systems with specific system codes are affected. Medical staff and patients using these systems may be at risk of incomplete imaging procedures.
Check if your system has one of the following system codes: 722064, 722222, 722230, or 722280. These codes are specific to the Azurion 3 M15 X-ray systems sold only in the United States of America.
Identify your system code by checking the system serial number or UDI (Unique Device Identifier) on the device.
The wired foot switch may fail to initiate X-ray imaging or cause intermittent imaging, potentially leading to incomplete medical procedures.
Check if your system has one of the system codes: 722064, 722222, 722230, or 722280. These codes are specific to the Azurion 3 M15 X-ray systems sold only in the United States of America.
The recall does not specify a remedy, so contact Philips directly for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1674-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1674-2026 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.
