MC2 Portable X-Ray System Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Oxos Medical Inc is recalling 77 MC2 and MC2.1 Portable X-Ray Systems due to a defective circuit board that overheats.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 18, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Oxos Medical Inc is recalling certain MC2 Portable X-Ray Systems because of a defective circuit board that overheats.
Which Products Are Affected
The recall involves the MC2 Portable X-Ray System (models MC2 and MC2.1, software version 5.7.0). A total of 77 units are affected, distributed nationwide in the states of FL, GA, IN, SC, TX, and VA. Affected serial numbers are: MC2 (1523, 1527, 1488, 1528, 1529, 1544) and MC2.1 (1461, 1462, 1547). Full UDIs and lot codes are provided in the recall notice.
What You Should Do
Consumers should follow instructions provided in the firm's notification letter regarding the recalled devices.
Why This Matters
This Class II recall involves a device used for diagnostic x-rays of extremities and shoulders, with potential for overheating due to the circuit board defect.
Source
FDA recall number Z-2857-2026. https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (903 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 18, 2026.
Frequently Asked Questions
Common questions about this FDA recall.