V. Mueller CH8610Recalls & reported problems
Steris Corporation · V. Mueller JACOBSON MOSQUITO FORCEPS CURVED JAWS DELICATE OVERALL LENGTH 5 inches 12.7CM · Class 1
- 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 10885403035364), received between Apr 24, 2026 and Apr 24, 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 24, 2026Break
THE USER FACILITY REPORTED VIA MEDWATCH # (B)(4) "AT THE END OF A PEDIATRIC HERNIA REPAIR, THE STAFF IDENTIFIED A FORCEPS INSTRUMENT HAD A BROKEN TIP. THE SURGEON WAS QUESTIONED AND THEY WERE CERTAIN THAT THEY DIDN'T USE THIS SPECIFIC FORCEPS FOR THE PROCEDURE AND THAT IT MUST HAVE BEEN THAT WAY BEFORE THEY STARTED. TO BE SAFE, LEADERSHIP ASKED THE TEAM TO DO AN X-RAY IN WHICH IT CAME BACK WITH NOTHING LEFT BEHIND."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24980906 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.