MicroFrance® CEV134BGRecalls & reported problems
Integra Microfrance · MicroFrance® Gayet bipolar forceps, fenestrated jaws, 5 mm diameter, 360 mm length, graduated tube 100 mm, ergonomic handle · Class 2
All models of MicroFrance (22)
Data updated Oct 16, 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 10381780091844), received between Dec 3, 2024 and Dec 3, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 3, 2024Break; Break
IT WAS REPORTED THAT THE CLAMP/360MM GAYET BIPOLAR FORCEPS (CEV134BG) "BROKE AT THE HANDLE WHERE THE SCREW WAS UNSCREWED AND WAS GONE". THE CLAMP REPORTEDLY BROKE IN THE PATIENT. THERE WAS NO CONSEQUENCES TO THE PATIENT BUT AN UNSPECIFIED DELAY IN CARE OCCURRED. WHEN ASKED IF THE PROCEDURE WAS COMPLETED USING A ANOTHER DEVICE OR METHOD, CUSTOMER REPLIED THAT THEY HAVE A STOCK OF TWEEZERS THAT THEY HAVE SET UP FOLLOWING BREAKAGES. IT WAS NOT REPORTED WHETHER ALL PARTS WERE RETRIEVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20832681 ↗
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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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