FDA Adverse Event Injury Summary report: N

AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - POSTERIOR

MDR report key: 3213409 · Received July 3, 2013

Report

Report Number
1018233-2013-02732
Event Type
Injury
Date Received
July 3, 2013
Report Date
June 8, 2018
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
TX, 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 OG 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

(B)(4). THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT NOT YET RECEIVED. ASSOCIATED MDR: 1018233-2013-02734.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
304933 AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - POSTERIOR MESH, SURGICAL, POLYMERIC FTL C.R. BARD, INC. (COVINGTON) NA CVRJ0026

Patients

Seq Age Sex Outcome Treatment
1 34 YR Female Required Intervention 486101, LOT #CVRI0039| AVAULTA PLUS ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM:| LYNX SLING: 850300| LYNX SLING: 850300| AVAULTA PLUS ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM:| 486101, LOT #CVRI0039