V. Mueller CV5050Recalls & reported problems
Steris Corporation · FOGARTY HYDRAGRIP CLAMP ANGLED JAWS ACCEPT 86MM INSERTS OVERALL LENGTH 9-1/4 inches23.5CM · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885403036354), received between Jul 11, 2025 and Apr 23, 2026 — classified as 2 malfunctions.
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
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR FOGARTY HYDRAGRIP CLAMP BROKE. ANOTHER CLAMP WAS USED TO COMPLETE THE PROCEDURE WHICH RESULTED IN A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24969255 ↗MalfunctionJul 11, 2025Break; Break
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR FOGARTY HYDRAGRIP CLAMP BROKE. ANOTHER CLAMP WAS USED TO COMPLETE THE PROCEDURE WHICH RESULTED IN A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22482347 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.