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Cook G08665Recalls & reported problems

Cook Incorporated · Peripherally Inserted Central Venous Catheter Set Silicone · Class 2 · Implant

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 00827002086654), received between Apr 19, 2018 and Apr 19, 2018 — classified as 1 malfunction.

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

  • Leak/Splash1

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.

  • MalfunctionApr 19, 2018Leak/Splash; Leak/Splash

    IT WAS REPORTED A DOCTOR NOTICED THE DOUBLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET WAS LEAKING THIRTEEN DAYS AFTER PICC PLACEMENT AT THE LARGE LUMEN AFTER HE HAD CLAMPED THE LINE PROXIMAL TO THE HOLE. AS REPORTED, THE DOCTOR ASSUMES THE CLAMP CAUSED THIS LEAK, HOWEVER, THE DEVICE REMAINS IN THE PATIENT AS HE IS STILL USING THE SMALL LUMEN OF BY THE LARGE LUMEN OF THE CATHETER. AS REPORTED, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS OR REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7444755 ↗

Other Catheter,intravascular,therapeutic,short-term less than 30 days devices

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Sources and updates

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