Many hernia mesh victims are seeking pertinent information about hernia mesh PerFix Plug lawsuits. Perflex Plug is a type of hernia mesh manufactured by Bard in conjunction with their subsidiary Davol. Perfix Plug hernia mesh is a Monofilament Knitted Polypropylene mesh. It is primary used for hernia repair.

Perfix

Perfix plug hernia MESH LAWSUIT

This mesh has become infamous for severe complications including: “mesh erosion, extrusion/protrusion, chronic pain, mesh contraction, infection, abscesses, fistulae, inflammation, scar tissue, organ perforation, dyspareunia, bleeding, neuropathy, and other acute and chronic nerve damage and pain, pelvic pain, prolapse of organs, and in most cases forcing the need for intensive medical treatment, including but not limited to operations to locate and remove mesh, operations to attempt to repair pelvic organs, tissue and nerve damage, the use of pain control and other medications, injections into various areas of the pelvis and spine.” PLAINTIFF’S ORIGINAL COMPLAINT & JURY DEMAND

Bard PerFix Light Plug recall

Another Perfix plug, the Bard PerFix Light Plug was recalled in an FDA Class 2 device recall  “The Bard PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects”  Class 2 Device Recall Bard PerFix Light Plug

PerFix Plug Lawsuit

Many victims are wondering if there will be a global Perflix Plug lawsuit settlement 2017 or if any Perflix Plug lawsuits will be settled in 2018. Some aggrieved surgical mesh victims are trying to determine if the is an average settlement amount for hernia mesh lawsuits. There are no clear answer to these questions. Top hernia mesh attorneys are litigating these causes of action against Bard/ Davol seeking justice and compensation for victims.

Matthew Ochoa recently filed a lawsuit complaint against Defendants C.R. BARD, INC. and BARD DAVOL, INC. This lawsuit alleges in pertinent part that:

  • “the Bard Defendants manufactured, promoted, distributed and sold for profit a product entitled BARD Perfix Plug Large-6/CTN Catalogue Number 0112970 GTIN 1080174106874 (“Bard Perfix Mesh”). Defendant promoted, distributed, and sold the Bard Perfix Mesh, as a product to repair hernia surgeries in the population. Defendant BARD describes the product as follows, “The Bard PerFix Plug is ideal for use in a tension-free preperitoneal repair technique. Since its introduction in 1993, it has been used in more than four million implants worldwide and has kept pace with new surgical techniques.” PLAINTIFF’S ORIGINAL COMPLAINT & JURY DEMAND, Paragraph #26, UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF TEXAS HOUSTON DIVISION, MATTHEW OCHOA, Plaintiff,V. C.R. BARD, INC., BARD DAVOL, INC., JOHNSON & JOHNSON, ETHICON, INC., ETHICON US, LLC, AND ETHICON ENDO-SURGERY, INC., Defendants.
  • “At all times relevant hereto, the Defendant knew of the defective nature of its product and its labeling as herein set forth, yet continued to design, manufacture, market, distribute and sell its product to maximize sales and profits at the expense of the general public’s health and safety in conscious disregard for the foreseeable harm caused by this product. Defendant’s conduct exhibited such an entire want of care as to establish that its actions were a result of fraud, ill will, recklessness, gross negligence or willful and intentional disregard to the Plaintiff’s individual rights, health and well-being and hence punitive damages are appropriate.” Id.

 

What are the alleged defects to the Perfix Plug alleged in the Ochoa lawsuit:

“a. The material is not inert and therefore reacts to human tissues and/or other naturally
occurring human bodily contents adversely affecting patient health.
b. The mesh material harbors infections that adversely affect human tissues and
patient health.
c. The mesh products migrate from the location of their implantation, adversely
affecting tissues and patient health.
d. If polypropylene, the mesh material abrades tissues adversely affecting patient
health.
e. The pelvic mesh products regularly fail to perform the purpose of their implantation
such that the patient requires removal of the device and repeated treatment and
surgery.
f. Due to their various defects, the pelvic mesh products regularly cause significant
injury to patients such that the mesh products must be removed, resulting in
additional surgery.
g. The mesh products become embedded in human tissue over time such that if it
needs to be removed due to its various defects, the removal causes damage to the
organs and tissues, adversely affecting patient health.
h. The mesh products are defective in shape, composition, weight, physical, chemical
and mechanical properties and are inappropriately engineered.
i. The mesh products erode into other pelvic organs, tissue, muscle, nerves, and bone
adversely affecting tissues and patient health.
j. The Defendants designed and defected an unreasonable dangerous hernia mesh
product.
k. Failed to adequately research the mesh.
l. The Defendants knew or should have known about the potential risk of infections,
allergic reactions, bowel damage and other internal injuries but withheld his
information from patients and doctors.
m. Defendants failed to properly investigate reports of problems after the hernia mesh
was introduced.
n. Defendants failed to warn about the risk of injury.
o. Defendants failed to promptly issue a recall after the problems were discovered.” Id.

Adverse event report:

DAVOL, C.R. BARD BARD MESH PERFIX PLUG, SIZE MEDIUM Back to Search Results
Lot Number 43KMD059 ??
Event Date 12/22/2010
Event Type  Injury
Event Description
Had a bard mesh perfix plug implanted to repair a right inguinal hernia in 2003. Experienced occasional excruciating pain and swelling after the recommended healing time passed, but was told by surgeon that healing can take a long time after surgery. As time went on, the pain became more and more frequent until it was so intolerable i knew something was very wrong. I was seen by another surgeon on (b)(6) 2010 and was schedule for corrective surgery the following day. I was told that the original mesh plug became detached from the muscle on one end and had folded up causing the intestine to poke through the opening and eventually get stuck. This resulted in the need for immediate corrective surgery to prevent bowel strangulation. The problem, i may be faced with now post surgery is possible permanent pain/discomfort/numbness from pubic area to thigh due to nerve damage. I’ve read reports from many other pts who experienced identical problems with this mesh plug; therefore, it is my hope that this plug will soon be added to the recall list to prevent future pts from having to experience these problems after hernia surgery.

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/Detail.CFM?MDRFOI__ID=1976659

If you are in need of legal representation contact us for a free review of your potential Perfix Plug claim. These cases will not be litigated as class actions. We are strongly opposed to class actions because individual surgical mesh victims do not have control over their case and whether they should settle. If the hernia mesh claim is accepted by a top hernia mesh law firm, the claim will be an individual lawsuit seeking justice and compensation.

Perfix Plug currently on the market:

Material Description Packaging
DVL0112750 MESH, PERFIX PLUG, SMALL, 1″X1.35″ 2/CS
DVL0112750H MESH, PERFIX PLUG, SMALL, 1″X1.35″ 1 EA
DVL0112760CS MESH PLUG MED -ORDR QTY 2 2/CS
DVL0112760H MESH PLUG MED 1 EA
DVL0112950 MESH, PERFIX PLUG, SMALL, 1″X1.35″ 6/CS
DVL0112960 MESH, PERFIX PLUG, MEDIUM, 1.3″X1.55″ 6/CS
DVL0112970 MESH, PERFIX PLUG, LARGE, 1.6″X1.9″ 6/CS
DVL0112980 MESH, PERFIX PLUG, XLG, 1.6″X2″ 6/CS
DVL117080 PLUG, PERFIX, XLG 1.5X2IN 1/CS