FDA Adverse Event Injury Summary report: N

XENFORM SOFT TISSUE REPAIR MATRIX

MDR report key: 6015179 · Received October 10, 2016

Report

Report Number
3005099803-2016-03027
Event Type
Injury
Date Received
October 10, 2016
Report Date
September 23, 2016
Manufacturer
BOSTON SCIENTIFIC - MARLBOROUGH
Product Code
PAJ
PMA / PMN Number
K060984
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

AS REPORTED BY THE PATIENT'S ATTORNEY, A BOSTON SCIENTIFIC DEVICE WAS IMPLANTED. ACCORDING TO THE COMPLAINANT, THE PATIENT EXPERIENCED AN UNKNOWN INJURY. ALL OTHER INFORMATION IS UNKNOWN. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
665159 XENFORM SOFT TISSUE REPAIR MATRIX MESH, SURGICAL, NON-SYNTHETIC, UROGYNECOLOGIC FOR APICAL VAGINAL AND UTERINE PRO PAJ BOSTON SCIENTIFIC - MARLBOROUGH UNK166

Patients

Seq Age Sex Outcome Treatment
1 Other