Konica Minolta recalls ImagePilot software versions 1.92 and 1.93 for medical imaging systems due to potential incorrect length/area calculations if power sequence is incorrect. Affected units include specific product and software versions.
lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel potential risk of incorrect length measurement/area calculation if incorrect power sequence is followed
Konica Minolta is recalling ImagePilot software versions 1.92 and 1.93 used in medical imaging systems. The software could produce incorrect length or area measurements if users follow the wrong power sequence, which might affect medical diagnoses.
The software versions 1.92 and 1.93, when paired with AeroDR or Momentum Panel hardware, may calculate incorrect lengths or areas if the power sequence is not followed properly. This could lead to inaccurate medical measurements that might impact patient care decisions.
Healthcare facilities using Konica Minolta ImagePilot software versions 1.92 or 1.93 for medical imaging systems are affected. Medical professionals who rely on these software versions for diagnostics are most at risk.
Check for product numbers ADFR or ADJC and software versions 1.92 or 1.93. Serial numbers listed in the recall include 996TDF3, F6H9BZ2, and others. UDI numbers for version 1.92 start with 04560141949492 and for 1.93 start with 04560141949584.
Verify your software version by checking the product documentation or the device settings.
Install the latest software update from Konica Minolta to correct the issue.
The software versions 1.92 and 1.93 could produce incorrect length or area measurements if the power sequence is not followed properly, potentially affecting medical diagnoses.
Check for product numbers ADFR or ADJC and software versions 1.92 or 1.93. Serial numbers listed in the recall include 996TDF3, F6H9BZ2, and others.
Yes, installing the latest software update from Konica Minolta will correct the issue.
We’ve drafted a message you can send Konica Minolta to request your refund or repair — edit it as you like.
Subject: Recall Z-0500-2022 — Konica Minolta Konica Minolta Hello, I own a Konica Minolta that is covered by recall Z-0500-2022 from Konica Minolta. 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.
