# FDA recall Z-2857-2026

> **Oxos Medical Inc** · Class II · device recall initiated 2026-06-11.

## Product

Brand Name: OXOS Medical, Inc  Product Name: MC2 Portable X-Ray System  Model/Catalog Number: MC2, MC2.1  Software Version: 5.7.0  Product Description: The MC2 Portable X-Ray System ( MC2 System  or  MC2 ) is a portable and handheld x-ray system designed to aid clinicians with point of care visualization through diagnostic x-rays of extremities and shoulders. The device allows a clinician to select desired technique factors best suited for their patient anatomy. The MC2 consists of two major system components: the emitter and the cassette. The MC2 emitter and cassette are battery-powered and can be charged with either a wired or wireless charger. The system is intended to interface wirelessly to an external tablet or display when used with the OXOS Device App. The MC2 utilizes an infrared Tracking System and Viewfinder that allows the operator to position the emitter within a safe source-to-image distance (SID) and allows the operator to visualize the anatomy and x-ray field projection prior to initiating an x-ray acquisition. The MC2 also utilizes a LIDAR system to ensure patient safety by maintaining a safe source-to-skin distance.  Component: The MC2 Portable X-Ray System is not a component.

## Reason for recall

Due to a defective circuit board that overheats

## Distribution

US Nationwide distribution in the states of FL, GA, IN, SC, TX, VA.

## Key facts

- **Recall number:** Z-2857-2026
- **Recalling firm:** Oxos Medical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-11
- **Report date:** 2026-08-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2857-2026

## Citation

> AI Analytics. FDA recall Z-2857-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2857-2026. Source: US FDA. Licensed CC0.

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