FDA recall, , Moderate risk
OXOS Medical MC2 Portable X-Ray System
The MC2 Portable X-Ray System has a defective circuit board that overheats.
Summary by Recall Canary from the FDA notice
What happened
Oxos Medical Inc of Atlanta, Georgia, began a recall on June 11, 2026, of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The FDA added the recall to its Enforcement Report on August 3, 2026. The system is a portable and handheld x-ray device for diagnostic x-rays of extremities and shoulders.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number and UDI-DI are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
MC2 Portable X-Ray System
- Model number
- MC2
- MC2.1
- UDI-DI
- 00860008892782
- 00850079606043
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Florida, Georgia, Indiana, South Carolina, Texas, Virginia.
- Company
- Oxos Medical IncAtlanta, Georgia
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99263
- Recall number
- Z-2857-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
