FDA Adverse Event Malfunction Summary report: N

REVEAL LINQ

MDR report key: 6319752 · Received February 9, 2017

Report

Report Number
9614453-2017-00795
Event Type
Malfunction
Date Received
February 9, 2017
Date of Event
November 23, 2016
Report Date
December 1, 2016
Manufacturer
IPG MFG SWITZERLAND
Product Code
DSI
PMA / PMN Number
K132649
Removal / Correction Number
Z-1249-2016
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: ANALYSIS INFORMATION -- (B)(6) 2016 18:25:13 CST PLI# 10 PRODUCT ID# LNQ11. THE DEVICE WAS NOT RETURNED FOR ANALYSIS. HOWEVER, PERFORMANCE DATA COLLECTED FROM THE DEVICE WAS RECEIVED AND ANALYZED. ANALYSIS OF THE DEVICE MEMORY INDICATED THE BATTERY IMPEDANCE TREND WAS RISING. RECOMMENDED REPLACEMENT TIME (RRT) ALERT WAS TRIGGERED ON (B)(6) 2016 DUE TO IMPEDANCE. DAILY BATTERY TREND DATA SHOWS GRADUAL RISE OF BATTERY IMPEDANCE. PREMATURE RRT ALERT, WITHOUT CORRESPONDING BATTERY DEPLETION. THIS DEVICE WAS REPORTED AS INCLUDED IN THE FIELD ACTION. BASED ON THE INFORMATION RECEIVED AND WITHOUT THE RETURN OF THE PRODUCT, IT CANNOT BE CONFIRMED THAT THIS DEVICE PERFORMED AS DESCRIBED IN THE FIELD ACTION. IT IS INCLUDED IN THE FIELD ACTION IN THE ABUNDANCE OF CAUTION.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE IMPLANTABLE CARDIAC MONITOR (ICM) DEVICE REACHED RECOMMENDED REPLACEMENT TIME (RRT) EARLIER THAN EXPECTED. THE DEVICE REMAINS IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
102797 REVEAL LINQ DETECTOR AND ALARM, ARRHYTHMIA DSI IPG MFG SWITZERLAND LNQ11

Patients

Seq Age Sex Outcome Treatment
1 57 YR