OXOS MC2 Portable X-Ray System: Defective Circuit Board Overheats
OXOS Medical recalls MC2 Portable X-Ray System models MC2 and MC2.1 with software version 5.7.0 due to a defective circuit board that overheats. Affected units have specific serial numbers and UDI codes listed in the recall notice.
Use caution until it’s fixed
Due to a defective circuit board that overheats
What happened, in plain English
OXOS Medical is recalling its MC2 Portable X-Ray System models MC2 and MC2.1 with software version 5.7.0 because a defective circuit board can overheat. This hazard could cause serious injury if the device is used improperly or left unattended. Read more at govinfonow.com/recall/314365-oxos-mc2-portable-x-ray-system-defective-circuit-board-overheats.
Source Summary by GovInfoNow · govinfonow.com/recall/314365-oxos-mc2-portable-x-ray-system-defective-circuit-board-overheats · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2857-2026
Cite this page
“OXOS MC2 Portable X-Ray System: Defective Circuit Board Overheats.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314365-oxos-mc2-portable-x-ray-system-defective-circuit-board-overheats. Based on FDA recall #Z-2857-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2857-2026%22&limit=1).
Why it’s dangerous
The defective circuit board overheats, which could lead to burns or fire if the device is left unattended or used in a way that causes excessive heat buildup. The system is designed for portable use but requires careful handling to prevent overheating.
Who’s affected
Healthcare providers using the MC2 Portable X-Ray System for point-of-care x-rays are most at risk. Patients receiving x-rays with affected devices may also be impacted.
How to tell if you have this one
Check for serial numbers 1523, 1527, 1488, 1528, 1529, 1544 (for MC2) or 1461, 1462, 1547 (for MC2.1). The device has a unique identifier (UDI) starting with 00860008892782 or 00850079606043.
- Brand
OXOS Medical- Product
Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software- Category
Medical device
What to do — step by step
Check Device Serial Number
Look for serial numbers listed in the recall notice: 1523, 1527, 1488, 1528, 1529, 1544 for MC2 models or 1461, 1462, 1547 for MC2.1 models.
Contact Manufacturer
Reach out to OXOS Medical for further assistance or to confirm if your device is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 6 states.
FDA distribution: “US Nationwide distribution in the states of FL, GA, IN, SC, TX, VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Georgia, Indiana, South Carolina, Texas, Virginia.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2857-2026 (June 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2857-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.