Turbo-Ject G49160Recalls & 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 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 00827002491601), received between Sep 15, 2017 and Sep 19, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Bent” (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
- Bent1
- Entrapment of Device1
- Inadequacy of Device Shape and/or Size1
- Torn Material1
Patient problems
- Injury1
- 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.
MalfunctionSep 19, 2017Entrapment of Device; Torn Material
DURING THE PROCEDURE THE OUTER PORTION OF THE PEELAWAY SHEATH TORE. THE OUTER END OF SHEATH PORTION TORE BECAUSE IT CAUGHT IN THE SKIN. A NEW DEVICE WAS USED TO COMPLETE THE PROCEDURE.
Patient problems: Injury
MAUDE report 6875081 ↗MalfunctionSep 15, 2017Bent; Inadequacy of Device Shape and/or Size
IT WAS REPORTED WHEN THE PACKAGE WAS OPENED, IT WAS NOTED THE GUIDE WIRE TIP WAS CURVED. DEVICE IMAGING IDENTIFIED COIL ELONGATION OF THE GUIDE WIRE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6867998 ↗
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- Groshong® Catheter 7717405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days279 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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