FDA Adverse Event Malfunction Summary report: N

ATTAIN ABILITY

MDR report key: 1991430 · Received February 15, 2011

Report

Report Number
2649622-2011-02391
Event Type
Malfunction
Date Received
February 15, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
OJX
PMA / PMN Number
P080006
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING THE IMPLANT ATTEMPT, THE LEAD DISLODGED FOLLOWING SLITTING. DUE TO THE PATIENT'S ANATOMY, THE PHYSICIAN OPTED NOT TO REPLACE THE LEAD IMMEDIATELY. THE LEAD WAS NOT IMPLANTED. 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 IMPLANTABLE PACING LEAD OJX MEDTRONIC PUERTO RICO, INC. 4196 ASKU

Patients

Seq Age Sex Outcome Treatment
1 78 YR Other