Philips recalls Azurion 7 B12 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 Azurion 7 B12 X-ray systems with system codes 722067, 722225, and 722235 because the X-ray imaging may not start or may stop intermittently when using the wired foot switch. This could lead to incomplete scans or repeated attempts to initiate imaging.
The X-ray imaging may not initiate or may stop intermittently when using the wired foot switch. This could cause incomplete scans or repeated attempts to start imaging, potentially leading to delays or errors in medical procedures.
Healthcare facilities using Philips Azurion 7 B12 X-ray systems with the specified system codes are most at risk. Patients and staff using these systems could experience incomplete imaging procedures.
Check for system codes 722067, 722225, or 722235 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 the device to confirm if it matches the recalled codes: 722067, 722225, or 722235.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Check the system code on your device. If it matches 722067, 722225, or 722235, contact Philips for further instructions.
The recall indicates potential for incomplete imaging, but no specific injuries have been reported. The risk is related to procedural errors rather than direct harm.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1675-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1675-2026 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.
