FDA Adverse Event Injury Summary report: N

AVAULTA PLUS SYNTHETIC SUPPORT SYSTEM: POSTERIOR

MDR report key: 2993832 · Received March 4, 2013

Report

Report Number
1018233-2013-00696
Event Type
Injury
Date Received
March 4, 2013
Report Date
November 11, 2015
Manufacturer
C.R. BARD, INC. (COVINGTON)
Product Code
FTL
PMA / PMN Number
K082571
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
ATTORNEY
Health Professional
N

Narratives

Additional Manufacturer Narrative · 1

THE SAMPLE WAS NOT RETURNED. THE FINISHED PRODUCT MET ALL SPECIFICATIONS PRIOR TO BEING RELEASED FOR GENERAL DISTRIBUTION. THE INSTRUCTIONS FOR USE WHICH ACCOMPANIES ALL DEVICES CURRENTLY ADDRESSES POTENTIAL RISKS ASSOCIATED WITH SURGICALLY IMPLANTED MATERIALS. THE INSTRUCTIONS FOR USE STATES IN THE ADVERSE REACTIONS: "POTENTIAL ADVERSE REACTIONS ARE THOSE TYPICALLY ASSOCIATED WITH SURGICALLY IMPLANTABLE MATERIALS, INCLUDING HEMATOMA, SEROMA, MUCOSAL OR VISCERAL EROSION, INFECTION, INFLAMMATION, SENSITIZATION, DYSPAREUNIA, SCARIFICATION AND CONTRACTION, FISTULA FORMATION, EXTRUSION AND RECURRENCE OF VAGINAL WALL PROLAPSE. PERFORATIONS OR LACERATIONS OF VESSELS, NERVES, BLADDER, BOWEL, RECTUM, OR ANY VISCERA MAY OCCUR DURING NEEDLE PASSAGE." (B)(4).

Description of Event or Problem · 1

THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT NOT YET RECEIVED. ASSOCIATED MDR: 1018233-2013-00697 AND 1018233-2013-00698.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
91631 AVAULTA PLUS SYNTHETIC SUPPORT SYSTEM: POSTERIOR Mesh, surgical, polymeric FTL C.R. BARD, INC. (COVINGTON) NA CVRH0024

Patients

Seq Age Sex Outcome Treatment
1 51 YR Female Required Intervention ALIGNTO URETHRAL SUPPORT SYSTEM| AVAULTA PLUS SYNTHETIC SUPPORT SYSTEM: ANTERIOR| ALIGNTO URETHRAL SUPPORT SYSTEM| AVAULTA PLUS SYNTHETIC SUPPORT SYSTEM: ANTERIOR