V. Mueller CH5707-3Recalls & reported problems
Steris Corporation · V. Mueller MIS SCISSORS - STRGLY CVD BLDS 5MM SHAFT, ROUND SQUEEZE HANDLE WORKING LENGTH 10 inches 25CM OVERALL LENGTH 14 inches 35.5CM · Class 2
All models of V. Mueller (118)
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 10885403181344), received between Dec 3, 2019 and Dec 3, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Jam” (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.
Most reported problems
Device problems
- Mechanical Jam1
- Mechanics Altered1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 3, 2019Mechanical Jam; Mechanics Altered
CH5707-3 MIS SCISSOR STRONGLY CURV - BAD PROBLEM WITH ERRATIC MOVEMENT AND STICKING CLOSED DURING CASE. AFTER CLEANING/SONICING THEY STILL DO NOT OPERATE SMOOTHLY. THE SURGEON STATED THAT HE FELT THE PATIENT DID NOT DO AS WELL DUE TO THE PROBLEMS THAT OCCURRED WITH THE INSTRUMENTATION. THE SCHEDULED PROCEDURE WAS TO REPAIR THE VALVE. THE REPAIR DID NOT HOLD, SO TRIED TO REWORK THE RING, AND ENDED UP REPLACING THE VALVE. THE SURGEON STRUGGLE WITH THE OPENING AND CLOSING OF INSTRUMENTS THE ENTIRE CASE. THIS RESULTED IN THE PATIENT BEING UNDER ANESTHESIA FOR A PROLONGED PERIOD OF TIME AND POSSIBLY AN UNNECESSARY PROCEDURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9406531 ↗
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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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