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.
Due to a defective circuit board that overheats
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.
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.
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.
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.
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.
Reach out to OXOS Medical for further assistance or to confirm if your device is affected.
The recall affects OXOS MC2 Portable X-Ray System models MC2 and MC2.1 with software version 5.7.0.
Check for serial numbers 1523, 1527, 1488, 1528, 1529, 1544 (for MC2) or 1461, 1462, 1547 (for MC2.1). The device also has a unique identifier (UDI) starting with 00860008892782 or 00850079606043.
The recall record does not specify a remedy, so affected users should contact OXOS Medical for further assistance.
We’ve drafted a message you can send OXOS Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2857-2026 — OXOS Medical OXOS Medical Hello, I own a OXOS Medical that is covered by recall Z-2857-2026 from OXOS Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
