FDA Adverse Event Injury Summary report: N

ATTAIN ABILITY PLUS

MDR report key: 3861154 · Received June 10, 2014

Report

Report Number
2649622-2014-07391
Event Type
Injury
Date Received
June 10, 2014
Date of Event
April 11, 2014
Report Date
April 11, 2014
Manufacturer
MPRI
Product Code
OJX
PMA / PMN Number
P080006
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY- THE FULL LEAD WAS RETURNED. ANALYSIS WAS PERFORMED AND NO ANOMALIES WERE FOUND.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. CONCOMITANT MEDICAL PRODUCTS: 6947M55 LEAD, (B)(6) 2013; 5076-45 LEAD, (B)(6) 2013. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CHRONIC LEFT VENTRICULAR (LV) LEAD DISLODGED FROM THE LATERAL VEIN OFF THE CORONARY SINUS. THE PHYSICIAN ATTEMPTED TO IMPLANT THE 1ST REPLACEMENT LV LEAD HOWEVER, IT DISLODGED FROM THE TARGET VESSEL AND WAS REMOVED AFTER MULTIPLE REPLACEMENT ATTEMPTS. THE PHYSICIAN ATTEMPTED TO IMPLANT THE 2ND REPLACEMENT LV LEAD HOWEVER, WAS NOT ABLE TO CANNULATE THE TARGET VESSEL. THE PHYSICIAN ATTEMPTED TO IMPLANT A 3RD LV LEAD HOWEVER, WAS UNABLE TO CANNULATE THE TARGET VESSEL. THE PHYSICIAN PLANNED FOR AN EPICARDIAL PLACEMENT AT A LATER DATE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
340090 ATTAIN ABILITY PLUS DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE OJX MPRI 429688

Patients

Seq Age Sex Outcome Treatment
1 00047 YR Hospitalization| R D314TRM ICD