Mobius Imaging recalls AIRO Mobile CT System Model MobiCT-32 with software version 2.0.0.0 due to potential undetected scan errors. Affected units may not alert operators of a faulty tube current modulation feature after scans complete.
The Tube Current Modulation feature (Modulated Scans) is not working in AIRO systems with software version 2.0.0.0, and operators would not be able to detect this fault until after a scan is completed.
Mobius Imaging recalls its AIRO Mobile CT System Model MobiCT-32 with software version 2.0.0.0 because the tube current modulation feature may not work properly. This could lead to undetected scan errors after a scan is completed, potentially affecting medical imaging accuracy.
The tube current modulation feature in the AIRO system may not function correctly with software version 2.0.0.0. Operators would not detect this fault until after a scan is completed, which could lead to inaccurate medical imaging results.
Healthcare facilities using the AIRO Mobile CT System Model MobiCT-32 with software version 2.0.0.0 are most likely affected. Medical staff operating these systems could be at risk if the software issue causes undetected scan errors.
Check if your AIRO Mobile CT System has model number MobiCT-32 and software version 2.0.0.0. The recall specifically targets this software version for the MobiCT-32 model.
Verify your AIRO Mobile CT System's software version to see if it is 2.0.0.0.
This recall affects AIRO Mobile CT System Model MobiCT-32 with software version 2.0.0.0. If your system has this software version, you are affected.
The recall does not specify a remedy, so you should check with Mobius Imaging for further instructions if your system has software version 2.0.0.0.
Look for model number MobiCT-32 and software version 2.0.0.0 on your AIRO Mobile CT System.
We’ve drafted a message you can send Mobius Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-2991-2018 — Mobius Imaging Mobius Imaging Hello, I own a Mobius Imaging that is covered by recall Z-2991-2018 from Mobius 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.
