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Cook G06540Recalls & reported problems

Cook Incorporated · Clear Body Three-Way Stopcock High Pressure · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002065406), received between Aug 3, 2016 and Aug 3, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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

  • Fluid/Blood Leak1

Patient problems

  • Chemical Exposure1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 3, 2016Fluid/Blood Leak; Fluid/Blood Leak

    THE DEVICES ARE NOT WATERPROOF. THE RADIOLOGIST ENDS UP WITH THE CHIMIO ON HIS HANDS THEREFORE THE PATIENT HAS LESS TREATMENT. PER THE CUSTOMER COMPLAINT FORM:"LEAK OF PRODUCT". THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE.

    Patient problems: Chemical Exposure

    MAUDE report 5843864 ↗

Other ACCESSORIES, CATHETER devices

All ACCESSORIES, CATHETER devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.