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Turbo-Flo G13309Recalls & reported problems

Cook Incorporated · Turbo-Flo PICC Set Polyurethane Peripherally Inserted Central Venous Catheter · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00827002133099), received between Sep 14, 2017 and Jul 29, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Disconnect” (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 18, 2026.

Most reported problems

Device problems

  • Failure to Disconnect1
  • Fluid/Blood Leak1
  • Material Rupture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 29, 2022Fluid/Blood Leak; Material Rupture; Fluid/Blood Leak; Material Rupture

    IT WAS REPORTED THAT A TWIN TURBO-FLO DOUBLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER RUPTURED IN THE PATIENT FOLLOWING A PICC LINE INSERTION. THE CATHETER WAS PLACED IN THE RIGHT BASILIC VEIN OF THE PATIENT ON (B)(6) 2022. ON (B)(6) 2022, THE PICC LINE WAS REMOVED AND AN APPROXIMATELY 0.8CM TEAR WAS DISCOVERED NEAR THE MIDDLE OF THE CATHETER (AROUND 11CM FROM INSERTION SITE EXCLUDING THE HUB). THE CATHETER WAS THEN FLUSHED, AND A LEAK WAS CONFIRMED TO BE COMING FROM THE TEAR. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES OR EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15135796 ↗
  • MalfunctionSep 14, 2017Failure to Disconnect

    IT WAS REPORTED THAT AFTER 2 HOURS OF ALBUMIN INFUSION, THE IV INFUSION CONNECTOR COULD NOT BE DISCONNECTED AS IT WAS STUCK IN THE SMALLER LUMEN OF THE DOUBLE LUMEN PICC LINE. AS A RESULT, THE CONNECTOR WAS REQUIRED TO BE CUT OFF . AFTER THIS INCIDENT, ONLY THE LARGER LUMEN CAN BE USED. THE PATIENT DIDN'T REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. THE COMPLAINANT REPORTED THERE HAVE NOT BEEN ADVERSE EFFECTS TO THE PATIENT DUE TO THIS OCCURRENCE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6864224 ↗

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Sources and updates

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