MicroFrance® CEV229-4ARecalls & reported problems
Integra Microfrance · Monopolar Hook, Jaws Size 3 (pk 3) for CEV225A CEV229-1A CEV9229-1 CEV82291 · 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 10381780092544), received between Jul 8, 2025 and Jul 8, 2025 — 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.
MalfunctionJul 8, 2025Break; Break
IT WAS REPORTED THAT THE INSULATION TIP OF HOOK CEV229-4A 3PK N3 FOR HOOK HANDLE (CEV229-4A) COMPLETELY BROKE OFF DURING A SURGICAL PROCEDURE. THE TIP WAS RECOVERED. IT IS UNKNOWN WHETHER THE TIP FELL INTO THE SURGICAL SITE. NO PATIENT INJURY AND A MINIMUM SURGICAL INCREASE OF LESS THAN 30 MINUTES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22436345 ↗
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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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