Thuvera MD2300F-001635Recalls & reported problems
IPG Medical Corporation · Thuvera, Flat Tip, Single-Use Laser Fiber, 200um · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810071230035), received between Nov 21, 2025 and Nov 21, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Separation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 21, 2025Material Separation; Material Separation
IT WAS REPORTED THAT A FIBER TIP BROKE OFF IN PATIENT. THE PHYSICIAN TRIED TO BASKET OUT THE BROKEN PIECE OF FIBER BUT WAS NOT SUCCESSFUL. NEXT COURSE OF ACTION IS UNKNOWN. THERE WERE NO PATIENT COMPLICATIONS.
Patient problems: Foreign Body In Patient
MAUDE report 23613649 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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