FDA Adverse Event Injury Summary report: N

PICC LINE

MDR report key: 4190261 · Received October 13, 2014

Report

Report Number
MW5038688
Event Type
Injury
Date Received
October 13, 2014
Date of Event
September 2, 2014
Report Date
October 13, 2014
Manufacturer
BARD
Product Code
LJS
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

NEW PICC LINE PLACED AND NEEDED REPOSITIONED. DURING REPOSITIONING, GUIDEWIRE WAS RETAINED IN PATIENT'S ARM. PATIENT WENT TO (B)(6) THE NEXT DAY FOR SAFE REMOVAL OF THE RETAINED GUIDEWIRE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
647206 PICC LINE PICC LINE LJS BARD REYG0688

Patients

Seq Age Sex Outcome Treatment
1 43 YR Required Intervention