FDA Adverse Event Injury Summary report: N

AVAULTA SOLO POSTERIOR SYNTHETIC SUPPORT SYSTEM

MDR report key: 3113597 · Received May 9, 2013

Report

Report Number
1018233-2013-01861
Event Type
Injury
Date Received
May 9, 2013
Report Date
March 8, 2016
Manufacturer
BARD SHANNON LIMITED
Product Code
FTL
PMA / PMN Number
K082571
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, 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 INSTRUCTION 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

PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADD'L INFO HAS BEEN REQUESTED, BUT NOT YET REC'D. ASSOCIATED MDR: 1018233-2013-01860.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
204820 AVAULTA SOLO POSTERIOR SYNTHETIC SUPPORT SYSTEM Mesh, surgical, polymeric FTL BARD SHANNON LIMITED NA HUSK0106

Patients

Seq Age Sex Outcome Treatment
1 59 YR Female Required Intervention AVAULTA SOLO ANTERIOR SYNTHETIC SUPPORT SYSTEM| LYNX - BOSTON SCIENTIFIC| LYNX - BOSTON SCIENTIFIC| AVAULTA SOLO ANTERIOR SYNTHETIC SUPPORT SYSTEM