FDA Adverse Event Malfunction Summary report: N

12 FT. EXTENSION SET, EASY LOCK CONNECTOR

MDR report key: 254814 · Received December 13, 1999

Report

Report Number
1423500-1999-01497
Event Type
Malfunction
Date Received
December 13, 1999
Date of Event
November 26, 1999
Report Date
November 26, 1999
Manufacturer
BAXTER HEALTHCARE CORP.
Product Code
KDJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

HOME PT (HP) REPORTS "EXTREME" SHOULDER PAIN DUE TO EXCESS AIR. HP REPORTS SHE WAS NOT PRIMING HER PT 12 FT. EXTENSION SET PROPERLY. HP REPORTS THE PAIN HAS DISSIPATED AND NO MEDICAL INTERVENTION HAS BEEN NECESSARY. HP NOTES SHE NOTIFIED DR. AND NO X-RAY WAS TAKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 12 FT. EXTENSION SET, EASY LOCK CONNECTOR EXTENSION LINE KDJ BAXTER HEALTHCARE CORP. NA NA01

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG.