FDA Adverse Event Injury Summary report: N

DESARA

MDR report key: 3012383 · Received March 7, 2013

Report

Report Number
3003990090-2012-00227
Event Type
Injury
Date Received
March 7, 2013
Date of Event
April 26, 2010
Report Date
December 6, 2012
Manufacturer
CALDERA MEDICAL, INC.
Product Code
FTL
PMA / PMN Number
K072456
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

EVENT WAS REPORTED TO CALDERA MEDICAL BY AN ATTORNEY. LEGAL COMPLAINT STATES THAT PT SUFFERED BODILY INJURIES. INJURIES AND OR SYMPTOMS INCLUDE CHRONIC VAGINAL PAIN, ABDOMINAL PAIN, URINARY TRACT INFECTIONS AND PAINFUL SEXUAL INTERCOURSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
98448 DESARA SURGICAL MESH FTL CALDERA MEDICAL, INC. CAL-DS01 30007

Patients

Seq Age Sex Outcome Treatment
1 Other