FDA Adverse Event Injury Summary report: N

UPHOLD VAGINAL SUPPORT SYSTEM

MDR report key: 5541424 · Received April 1, 2016

Report

Report Number
3005099803-2016-00941
Event Type
Injury
Date Received
April 1, 2016
Report Date
March 3, 2016
Manufacturer
BOSTON SCIENTIFIC - MARLBOROUGH
Product Code
OTP
PMA / PMN Number
K081048
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(6). (B)(4). LITERATURE - EVENT PUBLISHED IN THE FOLLOWING JOURNAL ARTICLE: LETOUZEY, V., ULRICH, D., BALENBOIS, E., CORNILLE, A., DE TAYRAC, R., & FATTON, B. (2015). UTERO-VAGINAL SUSPENSION USING BILATERAL VAGINAL ANTERIOR SACROSPINOUS FIXATION WITH MESH: INTERMEDIATE RESULTS OF A COHORT STUDY. INTERNATIONAL UROGYNECOLOGY JOURNAL, 26(12), 1803-1807. HTTP://DX.DOI.ORG/10.1007/S00192-015-2748-Z

Description of Event or Problem · 1

PER THE PUBLISHED JOURNAL ARTICLE, AN UPHOLD VAGINAL SUPPORT SYSTEM WAS IMPLANTED INTO THE PATIENT FOR ANTERIOR/APICAL PELVIC FLOOR REPAIR ON AN UNSPECIFIED DATE BETWEEN 2009 AND 2013. ACCORDING TO THE ARTICLE, THE PATIENT REQUIRED MESH REVISION SURGERY FOR VAGINAL MESH EXPOSURE (WITHOUT COMPLETE REMOVAL OF THE MESH). FOLLOWING THE REVISION SURGERY, THE PATIENT HAD COMPLETE SYMPTOM RESOLUTION. 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
196579 UPHOLD VAGINAL SUPPORT SYSTEM MESH, SURGICAL, SYNTHETIC OTP BOSTON SCIENTIFIC - MARLBOROUGH M0068317080

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention