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Turbo-Ject G03789Recalls & reported problems

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

All models of Turbo-Ject (40)

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 00827002037892), received between Sep 18, 2017 and Sep 18, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unraveled Material” (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

  • Unraveled Material1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • MalfunctionSep 18, 2017Unraveled Material

    DURING A PICC INSERTION ON AN ONCOLOGY PATIENT, THE ETCHED WIRE WAS INSERTED INTO THE PATIENT TO MEASURE FOR PICC TRIMMING. HOWEVER, THE WIRE TIP UNRAVELED FROM ITSELF AND ANOTHER KIT HAD TO BE OPENED TO UTILIZE THE ETCHED WIRE. ASIDE FROM THE PICC LINE, NO PART OF THE DEVICE REMAINED INSIDE THE PATIENT.

    Patient problems: No Code Available

    MAUDE report 6874051 ↗

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Sources and updates

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