FDA Adverse Event Malfunction Summary report: N

TRUWAVE DISPOSABLE PRESSURE TRANSDUCER

MDR report key: 1082350 · Received July 24, 2008

Report

Report Number
6000002-2008-08179
Event Type
Malfunction
Date Received
July 24, 2008
Date of Event
July 2, 2008
Report Date
July 2, 2008
Manufacturer
EDWARDS LIFESCIENCES
Product Code
DRS
PMA / PMN Number
K925638
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE HAS NOT BEEN RECEIVED FOR EVALUATION.

Description of Event or Problem · 1

IT WAS REPORTED THE SNAP-TAB DEVICE WAS BROKEN. TO PATIENT LINE AND TO IV SET LINE ARE BOTH CUT BY THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRUWAVE DISPOSABLE PRESSURE TRANSDUCER DISPOSABLE PRESSURE MONITOR DRS EDWARDS LIFESCIENCES PX260 UNK

Patients

Seq Age Sex Outcome Treatment
1 UNK