Konica Minolta ImagePilot 1.92/1.93 Software Recall: Incorrect Length Measurement Risk
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.
Lower-risk recall
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
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What happened, in plain English
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. Read more at govinfonow.com/recall/61473-konica-minolta-imagepilot-1-92-1-93-software-recall-incorrect.
Source Summary by GovInfoNow · govinfonow.com/recall/61473-konica-minolta-imagepilot-1-92-1-93-software-recall-incorrect · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0500-2022
Cite this page
“Konica Minolta ImagePilot 1.92/1.93 Software Recall: Incorrect Length Measurement Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61473-konica-minolta-imagepilot-1-92-1-93-software-recall-incorrect. Based on FDA recall #Z-0500-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0500-2022%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Konica Minolta- Category
Medical device
What to do — step by step
Check Software Version
Verify your software version by checking the product documentation or the device settings.
Update Software
Install the latest software update from Konica Minolta to correct the issue.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.1 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0500-2022 (December 3, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0500-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.