MicroFrance® 702TRecalls & reported problems
Integra Microfrance · MicroFrance® Crile-Wood tungsten needle-holder, 150 mm · Class 1
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 10381780088301), received between Apr 1, 2026 and Apr 1, 2026 — 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. How this data works · Data updated Oct 13, 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.
MalfunctionApr 1, 2026Break
A FACILITY REPORTED THAT THEY LOST A PIECE OF THE NEEDLE HOLDER 702T 150MM CRILE WOOD (702T) DURING SUTURING OF AN EAR, NOSE, AND THROAT PROCEDURE. IT WAS REPORTED THAT THE FAILURE OCCURRED WITHOUT ANY TENSION BEING APPLIED TO THE NEEDLE HOLDER, AND THE THREAD WAS VERY THIN. THE FRAGMENT WAS RETRIEVED WITHOUT DIFFICULTY, AND NO X-RAY WAS NEEDED FOR CONFIRMATION. ANOTHER INSTRUMENT WAS USED TO COMPLETE THE PROCEDURE. NO PATIENT INJURIES, DEATHS, OR DELAYS IN SURGERY WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24760550 ↗
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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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