FDA Adverse Event Injury Summary report: N

MINICAP DISCONNECT CAP

MDR report key: 206381 · Received January 7, 1999

Report

Report Number
1423500-1999-00015
Event Type
Injury
Date Received
January 7, 1999
Date of Event
September 8, 1998
Report Date
December 11, 1998
Manufacturer
BAXTER HEALTHCARE CORP.
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

REGISTERED NURSE REPORTED A HOME PT WAS DIAGNOSED WITH PERITONITIS ON 09/08/1998 AND TREATED WITH ANTIBIOTICS. NO PRODUCT FAILURE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MINICAP DISCONNECT CAP MINICAP KDJ BAXTER HEALTHCARE CORP. NA NA01

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other