Ultra V UniBody Handpiece 1Recalls & reported problems
Alma Lasers Ltd. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 17290110120228), received between Mar 8, 2019 and Mar 8, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Burn(s)1
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 8, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
THE SUSPECTED DEVICE WAS USED ON THE PATIENT'S ABDOMEN. AS PER THE FACILITY, THE PATIENT REPORTED SHE HAS SUSTAINED A SMALL BURN 1 INCH TO THE RIGHT OF HER BELLY BUTTON. THE PATIENT CALLED IN TO REPORT THIS BURN TWO WEEKS AFTER THE TREATMENT.
Patient problems: Burn(s); Partial thickness (Second Degree) Burn
MAUDE report 8404853 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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