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Turbo-Ject G23713Recalls & 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
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 00827002237131), received between May 4, 2017 and May 5, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Defective Component” (2 reports).

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

  • Defective Component2

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

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

  • MalfunctionMay 5, 2017Defective Component; Defective Component

    INTERNATIONAL CUSTOMER REPORTED THAT A PATIENT UNDERWENT IMPLANT OF A TURBO-JECT® SINGLE LUMEN BEDSIDE POWER-INJECTABLE PICC. WHEN THE PATIENT RETURNED TO THEIR ROOM THE NURSE DISCOVERED THAT THE ONE-WAY VALVE WAS FAULTY DESCRIBED AS "IMPOSSIBLE TO PERFUSE OR REMOVE BLOOD." THE PATIENT WAS RETURNED TO THE RECOVERY ROOM WHERE THE DEVICE WAS TESTED. IT WAS DETERMINED THAT THE PICC LINE WAS FUNCTIONING PROPERLY, HOWEVER THE ONE-WAY VALVE FAILED TO FUNCTION. RADIOGRAPHS SHOWED THE PICC LINE PROPERLY PLACED. THE VALVE WAS REPLACED. THERE ARE NO REPORTED ADVERSE PATIENT CONSEQUENCES. THE DEVICE IS NOT AVAILABLE FOR EVALUATION.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6547207 ↗
  • MalfunctionMay 4, 2017Defective Component; Defective Component

    INTERNATIONAL CUSTOMER REPORTED THAT A PATIENT UNDERWENT IMPLANT OF A TURBO-JECT® SINGLE LUMEN BEDSIDE POWER-INJECTABLE PICC. WHEN THE PATIENT RETURNED TO THEIR ROOM THE NURSE DISCOVERED THAT THE ONE-WAY VALVE WAS FAULTY DESCRIBED AS "IMPOSSIBLE TO PERFUSE OR REMOVE BLOOD." THE PATIENT WAS RETURNED TO THE RECOVERY ROOM WHERE THE DEVICE WAS TESTED. IT WAS DETERMINED THAT THE PICC LINE WAS FUNCTIONING PROPERLY, HOWEVER THE ONE-WAY VALVE FAILED TO FUNCTION. RADIOGRAPHS SHOWED THE PICC LINE PROPERLY PLACED. THE VALVE WAS REPLACED. THERE ARE NO REPORTED ADVERSE PATIENT CONSEQUENCES. THE DEVICE IS NOT AVAILABLE FOR EVALUATION.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6544647 ↗

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Sources and updates

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