FDA Adverse Event Injury Summary report: N

AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR

MDR report key: 3240041 · Received July 18, 2013

Report

Report Number
1018233-2013-02869
Event Type
Injury
Date Received
July 18, 2013
Report Date
June 18, 2013
Manufacturer
BARD SHANNON LTD
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

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, WHICH MAY OCCUR DURING NEEDLE PASSAGE." (B)(4).

Description of Event or Problem · 1

COMPLAINT # (B)(6). THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFO HAS BEEN REQUESTED BUT NOT YET RECEIVED. ASSOCIATED MDR #S: 1018233-2013-02871 AND 1018233-2013-02870.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
333438 AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR FTL BARD SHANNON LTD NA HUSL0148

Patients

Seq Age Sex Outcome Treatment
1 70 YR Required Intervention LOT# HUSI2213| PRODUCT# 486100, LOT# HUSK0698| PELVITEX POLYPROPYLENE MESH: PRODUCT#486015,| AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR| LOT# PIK00167| ALIGN RS URETHRAL SUPPORT SYSTEM: PRODUCT#BRD300RS