PlainRecalls
FDA Devices Moderate Class II Terminated

AIRO Mobile CT System Model # MobiCT-32

Reported: September 26, 2018 Initiated: August 1, 2018 #Z-2991-2018

Product Description

AIRO Mobile CT System Model # MobiCT-32

Reason for Recall

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.

Details

Recalling Firm
Mobius Imaging, LLC
Units Affected
147
Distribution
US and foreign distribution.
Location
Shirley, MA

Frequently Asked Questions

What product was recalled?
AIRO Mobile CT System Model # MobiCT-32. Recalled by Mobius Imaging, LLC. Units affected: 147.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 26, 2018. Severity: Moderate. Recall number: Z-2991-2018.