FDA Adverse Event Injury Summary report: N

ATTAIN OTW

MDR report key: 1992686 · Received February 15, 2011

Report

Report Number
2649622-2011-02991
Event Type
Injury
Date Received
February 15, 2011
Manufacturer
MEDTRONIC PUERTO RICO, 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
TX, 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) DEVICE DID NOT MEET EXPECTED LONGEVITY.

Additional Manufacturer Narrative · 1

ASKU

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT WAS EXPERIENCING DIAPHRAGMATIC STIMULATION. THE LV AMPLITUDE WAS DECREASED "WITH GOOD RESULTS." NO FURTHER PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. IT WAS LATER REPORTED THE LEFT VENTRICULAR LEAD AND DEVICE WERE EXPLANTED AND REPLACED. THE DEVICE WAS RETURNED TO MANUFACTURER, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION. LATER REPORTED THE LEFT VENTRICULAR LEAD WAS EXPLANTED DUE TO "NON FUNCTIONAL."

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT WAS EXPERIENCING DIAPHRAGMATIC STIMULATION. THE LV AMPLITUDE WAS DECREASED "WITH GOOD RESULTS." NO FURTHER PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. THE LEFT VENTRICULAR LEAD AND DEVICE WERE EXPLANTED AND REPLACED. THE DEVICE WAS RETURNED TO MANUFACTURER, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 47 YR Hospitalization| R 6949 IMPLANTABLE TACHY LEAD| 6949 IMPLANTABLE TACHY LEAD| 5076 IMPLANTABLE PACING LEAD| 5076 IMPLANTABLE PACING LEAD