FDA Adverse Event Injury Summary report: N

ATTAIN ABILITY

MDR report key: 1855066 · Received October 5, 2010

Report

Report Number
2649622-2010-09254
Event Type
Injury
Date Received
October 5, 2010
Date of Event
August 12, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
OJX
PMA / PMN Number
P080006
Removal / Correction Number
ASKU
Report Source
Manufacturer report
Reporter Location
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. EVALUATION SUMMARY: (B)(4) NO ANOMALIES FOUND; FULL LEAD IN SEGMENTS RETURNED AND ANALYZED. NO EVIDENCE OF A FRACTURE WAS FOUND. THE LEAD APPEARED TO HAVE BEEN CUT IN TWO.

Description of Event or Problem · 1

IT WAS REPORTED THAT HIGH THRESHOLD WAS OBSERVED ON THE LEFT VENTRICULAR LEAD. DURING AN ATTEMPT TO REPOSITION THE LEAD, WHILE PULLING BACK WITH A "GENTLE TUG," THE LEAD BROKE. IT WAS EXPLANTED, AND A NEW LEAD WAS SUCCESSFULLY PLACED. 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 69 YR Required Intervention 4574 IMPLANTABLE PACING LEAD| 6935 IMPLANTABLE TACHY LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB