FDA Adverse Event Injury Summary report: N

PINNACLE PELVIC FLOOR REPAIR KITS

MDR report key: 2884605 · Received December 24, 2012

Report

Report Number
3005099803-2012-06190
Event Type
Injury
Date Received
December 24, 2012
Report Date
December 4, 2012
Manufacturer
BOSTON SCIENTIFIC - MARLBOROUGH
Product Code
FTL
PMA / PMN Number
K071957
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION RECEIVED: UPDATED.

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A PINNACLE POSTERIOR PELVIC FLOOR REPAIR KIT WAS IMPLANTED ON (B)(6) 2009. ACCORDING TO THE COMPLAINANT, POST-PROCEDURE, THE PATIENT PRESENTED WITH UNSPECIFIED COMPLICATIONS. ALL OTHER INFORMATION IS UNKNOWN.

Description of Event or Problem · 1

ACCORDING TO THE PHYSICIAN, POST PROCEDURE, THE PATIENT COMPLAINED OF INCONTINENCE. ALL OTHER INFORMATION IS UNKNOWN AND UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PINNACLE PELVIC FLOOR REPAIR KITS MESH, SURGICAL, POLYMERIC FTL BOSTON SCIENTIFIC - MARLBOROUGH M0068317100

Patients

Seq Age Sex Outcome Treatment
1 Other