FDA Adverse Event Injury Summary report: N

B BRAUN EPIDURAL CATHETER

MDR report key: 4888256 · Received June 26, 2015

Report

Report Number
MW5043449
Event Type
Injury
Date Received
June 26, 2015
Date of Event
June 4, 2015
Report Date
June 26, 2015
Manufacturer
B BRAUN
Product Code
CAZ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

CRNA ATTEMPTED TO PLACE EPIDURAL CATHETER. HOWEVER, SHE WAS UNABLE TO FEED EPIDURAL CATHETER THROUGH TUOHY NEEDLE PAST 9 CM. CATHETER WAS WITHDRAWN. CRNA NOTED 2 CM OF CATHETER TO BE ABSENT FROM END OF CATHETER. ANOTHER CRNA REPORTED A SEPARATE, BUT RECENT ISSUE IN WHICH SHE WAS UNABLE TO FEED CATHETER. ANOTHER KIT WAS OBTAINED AND ANOTHER CRNA WAS ABLE TO INSERT EPIDURAL WITHOUT ISSUE. LOT NUMBER UNKNOWN AS PACKAGING NOT SAVED. LOTS CURRENTLY IN OB (B)(4) (ONLY ONE LEFT).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
414960 B BRAUN EPIDURAL CATHETER B BRAUN CAZ B BRAUN

Patients

Seq Age Sex Outcome Treatment
1 28 YR