FDA Adverse Event Injury Summary report: N

ATTAIN OTW

MDR report key: 2811602 · Received October 31, 2012

Report

Report Number
2649622-2012-15670
Event Type
Injury
Date Received
October 31, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P010015/S012
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

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 THE LEFT VENTRICULAR LEAD HAD FRACTURED AND CAUSED INHIBITED PACING. THE LEAD WAS WAS REPLACED. NO PATIENT COMPLICATIONS WERE NOTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ATTAIN OTW IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 4194

Patients

Seq Age Sex Outcome Treatment
1 86 YR Hospitalization| R 0157 COMPETITOR IMPLANTABLE TACHY LEAD| 4086 COMPETITOR IMPLANTABLE PACING LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB