FDA Adverse Event Injury Summary report: N

ATTAIN ABILITY PLUS

MDR report key: 1990490 · Received February 15, 2011

Report

Report Number
2649622-2011-02022
Event Type
Injury
Date Received
February 15, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
ASKU
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE THRESHOLDS ON THE LEAD INCREASED. THE LEAD WILL BE MONITORED AND 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
1 ATTAIN ABILITY PLUS IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 4296 ASKU

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R