Microline 110-005DRecalls & reported problems
Microline Surgical, Inc. · ENTceps · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00811099011545), received between Jan 23, 2025 and Mar 19, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Intermittent Loss of Power” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Intermittent Loss of Power2
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 19, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
DURING A TONSILLECTOMY, THE DEVICE FAILED CUTTING DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21645638 ↗MalfunctionFeb 25, 2025Intermittent Loss of Power; Intermittent Loss of Power
WE HAVE 10 UNITS FORM THE SAME LOT NR. 406558. CLIENT COMPLAINTS THE THEY HAD TO PRESS HARDER THAN USUAL AND AFTER 3 TO 4 BEEPS THE POWER CUT OUT AND THEY HAD TO REACTIVATE. THIS HAPPENED ONLY WITH ENTCEPS LOT: 406558, THE SAME LOT AS WE ALREADY HAD THE SAME COMPLAINT FOR WITH REGARDS TO MFR REPORT#: 1223422-2025-00001.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21462808 ↗MalfunctionJan 23, 2025Intermittent Loss of Power; Intermittent Loss of Power
ENT NOT WORKING PROPERLY. SEALING FUNCTION NOT WORKING CONTINOUSLY. THEY HAVE DISCARDED THE FORCEPS AFTER USAGE. ANESTHESIA TIME WAS EXTENDED AND ANOTHER SET FROM A DIFFERENT LOT WAS USED SUCCESSFULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21218057 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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