FDA Device recall Z-0344-2023
MobiCT-32 AIRO Mobile CT Scanner, Cat
- FDA Device
- Class II
- terminated
- Published 2022-12-07
On 2022-12-07 the FDA classified a Class II recall of MobiCT-32 AIRO Mobile CT Scanner, Cat by Mobius Imaging, citing 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 monitori….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0344-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-11-18 |
| Published | 2022-12-07 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Mobius Imaging |
| Distribution | CO, TN, UT |
Product
MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1
Reason
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.
Identifiers
| code_info | UDI-DI 00869346000200 Serial Numbers AIRO-0124, AIRO-0145, AIRO-0288 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0344-2023%22
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