FDA Adverse Event Injury Summary report: N

ATTAIN ABILITY

MDR report key: 2203757 · Received August 11, 2011

Report

Report Number
2649622-2011-11733
Event Type
Injury
Date Received
August 11, 2011
Date of Event
May 5, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
OJX
PMA / PMN Number
P080006
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, 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 AN ATTEMPTED IMPLANT, THE LEFT VENTRICULAR LEAD BECAME DISLODGED. THE PHYSICIAN WAS UNABLE TO GET THROUGH THE SMALL VEINS. THE LEAD WAS NOT USED. PATIENT WAS DISCHARGED HOME AND REFERRED TO ANOTHER FACILITY FOR EPICARDIAL LEAD PLACEMENT AT A LATER DATE. 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 65 YR Hospitalization| R