STAT 2 S2V-60Recalls & reported problems
Conmed Corporation · STAT 2 PRIMARY ADMINISTRATIVE SET GRAVITY FLOW CONTROLLER · Class 2
- 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 30653405033015), received between Jun 13, 2017 and Jun 13, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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.
Most reported problems
Device problems
- Infusion or Flow Problem1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 13, 2017Infusion or Flow Problem; Infusion or Flow Problem
THE USER FACILITY REPORTED THE DEVICE WAS NOT ALLOWING FLUIDS/DRUGS TO DRIP PROPERLY. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Information
MAUDE report 6636866 ↗
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- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.