---
title: "MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomogra... — FDA record Z-0344-2023 | Is It on Recall"
description: "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 who"
url: https://isitonrecall.com/recall/fda-device-z-0344-2023-mobict-32-airo-mobile-ct-scanner-cat-no-mobict-32-mobile-computed-tomography-ct-system-software-vers/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1 — FDA record Z-0344-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 18, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class II
- **Recalling firm**: Mobius Imaging, LLC
- **Quantity**: 3
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0344-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0344-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI 00869346000200 Serial Numbers AIRO-0124, AIRO-0145, AIRO-0288 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic distribution to consignees in Colorado, Tennessee, and Utah.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Colorado](https://isitonrecall.com/state/colorado/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Dec 7, 2022
- **Recall initiation date**: Nov 18, 2022
- **Center classification date**: Nov 30, 2022
- **Termination date**: Feb 26, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0344-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mobius Imaging, LLC records](https://isitonrecall.com/brand/mobius-imaging-llc/)