PlainRecalls
FDA Devices Moderate Class II Terminated

MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1

Reported: December 7, 2022 Initiated: November 18, 2022 #Z-0344-2023

Product Description

MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1

Reason for Recall

Stryker received a report of a battery fire involving an Airo TruCT unit previously subjected to bypass charging. The firm is notifying customers with units whose battery monitoring systems were bypassed to charge the batteries; the batteries in these units require replacing.

Details

Recalling Firm
Mobius Imaging, LLC
Units Affected
3
Distribution
Domestic distribution to consignees in Colorado, Tennessee, and Utah.
Location
Shirley, MA

Frequently Asked Questions

What product was recalled?
MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1. Recalled by Mobius Imaging, LLC. Units affected: 3.
Why was this product recalled?
Stryker received a report of a battery fire involving an Airo TruCT unit previously subjected to bypass charging. The firm is notifying customers with units whose battery monitoring systems were bypassed to charge the batteries; the batteries in these units require replacing.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 7, 2022. Severity: Moderate. Recall number: Z-0344-2023.