Skip to content

Cook G04472Recalls & reported problems

Cook Incorporated · Plastic Multipurpose Tubing Adapter · Class 1

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 00827002044722), received between Aug 28, 2017 and Aug 28, 2017 — classified as 1 malfunction.

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

  • 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.

  • MalfunctionAug 28, 2017Fluid/Blood Leak; Fluid/Blood Leak

    THE INTERNATIONAL CUSTOMER REPORTED THAT THE WAS A LEAKAGE OF URINE WHICH OCCURRED AT THE JUNCTION BETWEEN THE CONNECTING PIECE AND THE BODY OF THE MULTIPURPOSE PLASTIC TUBING ADAPTER. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE, AND NO ADDITIONAL PROCEDURES WERE REQUIRED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6824943 ↗

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.