FDA Adverse Event Injury Summary report: N

CAPSURE SP

MDR report key: 2131244 · Received June 16, 2011

Report

Report Number
2649622-2011-10628
Event Type
Injury
Date Received
June 16, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P830061/S12
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, 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) A PARTIAL LEAD WAS RETURNED IN SEGMENTS AND ANALYSIS REVEALED THAT THE INNER INSULATION WAS BREACHED WITH METAL INDUCED OXIDATION. ALL CONDUCTORS HAD BLOOD/BODY FLUID (NOT OBSTRUCTED). THE OUTER INSULATION WAS MELTED AND PULLED APART (OVERSTRESS). THE INNER AND OUTER INSULATION HAD COSMETIC METAL INDUCED OXIDATION. THE OUTER INSULATION HAD COSMETIC ENVIRONMENTAL STRESS CRACKING, A WHITE SUBSTANCE ON IT, AND A COSMETIC DEPRESSION. THE LEAD WAS STRETCHED. (B)(4) A PARTIAL LEAD WAS RETURNED IN SEGMENTS AND ANALYSIS REVEALED NO ANOMALIES. IT WAS NOTED THAT THE PROXIMAL CONDUCTOR HAD BLOOD/BODY FLUID (NOT OBSTRUCTED). THE OUTER INSULATION WAS BREACHED CUT AND HAD A COSMETIC DEPRESSION. THERE WAS BLOOD IN/ON HELIX/LOBE MECHANISM AND MECHANISM (SLEEVE HEAD) AND THERE WAS APPARENT EXPLANT DAMAGE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE RIGHT ATRIAL AND RIGHT VENTRICULAR LEADS BOTH HAD NO CAPTURE AND LEAD FRACTURES. BOTH LEADS WERE EXPLANTED AND REPLACED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSURE SP IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 4524 ASKU

Patients

Seq Age Sex Outcome Treatment
1 68 YR Hospitalization| R ADDR01 IMPLANTABLE PULSE GENERATOR