SC710MSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00606509300773), received between Jun 21, 2026 and Jun 21, 2026 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 21, 2026Appropriate Device Problem Term/Code Not Available

  Provider alleges the consumer was at the hospital, receiving treatment in the Emergency room, he left the ER to go have a smoke break outside, he had some type of ointment and bandages on his skin and it's the current belief that an ash from the cigarette, or the hot part of the cigarette came into contact with his skin where the ointment/bandages were and started a fire.

  Patient problems: Burn(s)

  MAUDE report 25572220 ↗