FDA Adverse Event Injury Summary report: N

ATTAIN OTW

MDR report key: 1921535 · Received December 13, 2010

Report

Report Number
2649622-2010-12579
Event Type
Injury
Date Received
December 13, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P010015/S003
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, 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.

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): THE DEVICE WAS RETURNED, ANALYZED AND ANALYSIS OF THE DEVICE REVEALED NORMAL BATTERY DEPLETION.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT HAD A COMPLAINT ABOUT THEIR DEVICE ONLY LASTING 2 YEARS. THE PATIENT WAS ALSO CONCERNED WITH POTENTIAL COMPLICATIONS FROM A NEEDED LEAD REVISION TO GET LOWER THRESHOLDS. THE DEVICE AND LEAD REMAIN IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT HAD A COMPLAINT ABOUT THEIR DEVICE ONLY LASTING 2 YEARS. THE PATIENT WAS ALSO CONCERNED WITH POTENTIAL COMPLICATIONS FROM A NEEDED LEAD REVISION TO GET BETTER THRESHOLDS. THE LEAD REMAINS IN USE AND THE DEVICE WAS REMOVED. 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 PUERTO RICO, INC. 4193 ASKU

Patients

Seq Age Sex Outcome Treatment
1 65 YR Hospitalization| O| R 6947 IMPLANTABLE TACHY LEAD| 4076 IMPLANTABLE PACING LEAD| 6947 IMPLANTABLE TACHY LEAD| 4076 IMPLANTABLE PACING LEAD