FDA Adverse Event Injury Summary report: N

DESARA

MDR report key: 3012409 · Received March 7, 2013

Report

Report Number
3003990090-2013-00014
Event Type
Injury
Date Received
March 7, 2013
Date of Event
April 18, 2011
Report Date
January 28, 2013
Manufacturer
CALDERA MEDICAL, INC.
Product Code
PAH
PMA / PMN Number
UNK
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

EVENT WAS REPORTED TO CALDERA MEDICAL BY AN ATTORNEY. LEGAL COMPLAINT STATES THAT PT SUFFERED PAIN, URINARY PROBLEMS, BOWEL PROBLEMS, DYSPAREUNIA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
98437 DESARA SURGICAL MESH PAH CALDERA MEDICAL, INC. CAL-DS01 UNK

Patients

Seq Age Sex Outcome Treatment
1 Other