V. Mueller CH6622Recalls & reported problems
Steris Corporation · V. Mueller COOLEY MULTI-PURPOSE CURVED CLAMP, CVD JAWS, ANGLED SHANKS JAW DEEP 1-1/2X3/4 inches 3.8X1.9CM OVERALL LENGTH 8 inches 20.3CM · 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 10885403031939), received between Oct 16, 2025 and Oct 16, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 16, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR COOLEY MULTI-PURPOSE CURVED CLAMP WAS "ATTRIBUTING TO LOCALIZED BLEEDING".
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 23311341 ↗
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- Flo-Thru Intraluminal Shunt® FT-12125Synovis Life Technologies, Inc. · CLAMP, VASCULAR1 recall1 report
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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