Deerfield Imaging recalls iMRX MRI and Angiography Systems with specific part numbers due to potential X-ray tube failure from generator A100 power supply issues. Affected units may not produce X-rays during procedures.
There is a potential hardware error for the iMRX System with a generator A100. A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible
Deerfield Imaging recalls two specific models of MRI and angiography systems that could fail to produce X-rays during procedures due to a power supply issue. This risk affects medical facilities using these systems for imaging procedures.
The generator A100 power supply may fail above a specific voltage threshold, causing the X-ray tube to not receive required voltage. This prevents X-ray imaging during procedures, which could impact diagnostic accuracy and patient care.
Medical facilities using the iMRX MRI and Angiography Systems with part numbers 10094137 or 10094141 are most at risk. These systems are used in surgical settings for imaging procedures.
Check for part numbers 10094137 or 10094141 on the iMRX MRI and Angiography System. Affected units have serial numbers including 146792, 153374, 153642, 153793, 153896, or 154588.
Identify if your iMRX system has part numbers 10094137 or 10094141.
Reach out to Deerfield Imaging for guidance on next steps if your system is affected.
The generator A100 power supply may fail above a specific voltage threshold, causing the X-ray tube to not receive required voltage and preventing X-ray imaging during procedures.
Part numbers 10094137 and 10094141 for the iMRX MRI and Angiography System.
Yes, serial numbers 146792, 153374, 153642, 153793, 153896, and 154588 are affected.
We’ve drafted a message you can send Deerfield Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-0762-2020 — Deerfield Imaging Deerfield Imaging Hello, I own a Deerfield Imaging that is covered by recall Z-0762-2020 from Deerfield Imaging. 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.
