FDA Adverse Event Injury Summary report: N

ATTAIN OTW

MDR report key: 2131956 · Received June 16, 2011

Report

Report Number
2182208-2011-00929
Event Type
Injury
Date Received
June 16, 2011
Date of Event
January 17, 2011
Manufacturer
MEDTRONIC, INC.
Product Code
DTB
PMA / PMN Number
P010015/S012
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PL
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS INFORMATION IS BASED ENTIRELY ON JOURNAL LITERATURE. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS LIMITED DUE TO CONFIDENTIALITY CONCERNS. THIS EVENT OCCURRED OUTSIDE THE U.S. WITHOUT A LOT NUMBER OR DEVICE SERIAL NUMBER, THE MANUFACTURING DATE CANNOT BE DETERMINED. SINCE NO DEVICE ID WAS PROVIDED, IT IS UNKNOWN IF THIS EVENT HAS BEEN PREVIOUSLY REPORTED. REFERENCED ARTICLE: " LEFT VENTRICULAR LEAD IMPLANTATION AT A PHRENIC STIMULATION SITE IS SAFE AND EFFECTIVE." EUROPACE. APRIL 1 2011;13(4):520-525.

Description of Event or Problem · 1

A JOURNAL ARTICLE WAS REVIEWED THAT CONTAINED INFORMATION REGARDING THIS LEAD. MULTIPLE FAILURE MODES WERE NOTED IN THE ARTICLE, HOWEVER A ONE TO ONE CORRELATION COULD NOT BE MADE WITH UNIQUE LEAD/SERIAL NUMBERS. THE ARTICLE INCLUDED THE FOLLOWING FAILURE MODES: UNACCEPTABLE THRESHOLDS, PHRENIC STIMULATION, PROGRAMMING DIFFICULTIES, AND IMPLANT ATTEMPTS DUE TO PATIENT ANATOMY. LEAD STATUS IS UNKNOWN. FURTHER FOLLOW-UP DID NOT YIELD ANY ADDITIONAL RELEVANT INFORMATION REGARDING THIS EVENT. 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 OTW IMPLANTABLE PACING LEAD DTB MEDTRONIC, INC. 4194 ASKU

Patients

Seq Age Sex Outcome Treatment
1 63 YR Hospitalization| R