FDA Adverse Event Injury Summary report: N

V-CATH PICC

MDR report key: 394456 · Received March 29, 2002

Report

Report Number
2925153-2002-00005
Event Type
Injury
Date Received
March 29, 2002
Date of Event
February 19, 2002
Report Date
March 19, 2002
Manufacturer
HDC CORPORATION
Product Code
DQO
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

CATHETER HAD BEEN INSERTED AND THEN FRACTURED RESULTING IN THE PT GOING BACK TO THE THEATRE TO HAVE THE LINE REMOVED, BUT PART OF THE LINE CAN NOT BE REMOVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 V-CATH PICC 2FR CATHETER DQO HDC CORPORATION 350-78 UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention