FDA Adverse Event Malfunction Summary report: N

10 LEAD ECG TRUNK AAMI/IEC 2M

MDR report key: 3897057 · Received May 16, 2014

Report

Report Number
9610816-2014-00130
Event Type
Malfunction
Date Received
May 16, 2014
Report Date
April 23, 2014
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
DSA
PMA / PMN Number
K020531
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4): A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE FAILURE OF AN M1663A ECG TRUNK CABLE. THERE WAS NO REPORT OF PATIENT HARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
294760 10 LEAD ECG TRUNK AAMI/IEC 2M DSA PHILIPS MEDICAL SYSTEMS M1663A 1B

Patients

Seq Age Sex Outcome Treatment
1