Covidien Progrip Hernia Mesh Lawsuit | Now Viable lawsuits!

This article by a hernia mesh lawsuit lawyer is about Covidien Parietex Progrip hernia mesh and Progrip hernia mesh lawsuits. There is no Progrip class action. There is no Progrip hernia mesh recall at this time.  Covidien progrip lawsuits can now be filed in the Massachusetts consolidated State Court proceedings as well as the Federal Court MDL in Massachusetts. More info about all Covidien hernia mesh lawsuits. A Progrip hernia mesh lawsuit lawyer can help an individual or family file a Progrip Mesh lawsuit to seek the financial damages they deserve. It’s important that you speak with an experienced Progrip hernia mesh lawsuit attorney as soon as possible to receive a free case evaluation. The time available to file a claim is limited by law. “Parietex ProGrip® (MedtronicsTM) is a bicomponent mesh comprising of monofilament polyester and a semi re-absorbable polylactic acid gripping system that allows sutureless fixation of prosthetic mesh to the posterior inguinal wall.” Pub Med

Progrip hernia mesh lawsuits

The following questions are answered:

• Is a Progrip Hernia Mesh Lawsuit the answer?
• Should you pursue a Covidien Progrip hernia mesh lawsuit?

Should you pursue a progrip lawsuit?

• Filing a hernia mesh Progrip lawsuit may be a viable option for anyone that has been injured or suffered severe complications related to the Parietex Progrip Mesh.
• Progrip hernia mesh is a popular hernia device.
• Progrip is a composite mesh that is sometimes used to support surrounding tissues during hernia repair surgery.
• It is believed that implanting Progrip Mesh can reduce the likelihood of a hernia recurrence.
• Nevertheless, many patients still suffer complications ranging from hernia recurrence to adhesion and infection.

Covidien previously entered into a statute of limitation tolling agreements with some lawyers extending the statute of limitations while settlement talks were ongoing. Covidien rescinded the tolling agreements.  Hernia mesh law firms are typically unwilling to file individual lawsuits unless damages are catastrophic and the value of the case is in the millions. Progrip is not under a recall.

Update- 2/24/2022- “Covidien LP and affiliated companies asked the U.S. Judicial Panel on Multidistrict Litigation for the second time to combine hernia mesh product liability suits, saying circumstances have dramatically changed since its first request for a multidistrict proceeding was denied in 2020. The suits should be combined and sent to the U.S. District Court for the District of Massachusetts, Covidien said.” Bloomberg law

August 2021– Covidien is in the process of cancelling the Covidien tolling agreements in the near future and has notified counsel of the victims. It will no longer be feasible to file monofilament mesh products in the Massachusetts state court proceedings.

Definition of a Hernia

A hernia diagnosis occurs when an intestine, bodily organ or some other soft tissue breaks through a weak area in the network of muscle and connective tissue in the areas of the abdomen or groin. More than 200,000 people are diagnosed annually with a hernia in the United States. The United States Food and Drug Administration has determined that a majority of hernias result from excessive abdominal pressure. The following factors can also contribute to the development of a hernia:

• Obesity
• Heavy lifting
• Diarrhea and constipation
• Coughing and sneezing
• Poor nutrition
• Smoking
• Overexertion

Hernia Mesh

There are more than a million surgical hernia repair procedures performed every year in the United States. Surgeons frequently employ a surgical patch or mesh to reduce the possibility of a hernia recurrence. Unfortunately, hernia recurrences are quite common. Hernia mesh is often manufactured from a variety of synthetic materials, including ePTFE, polyester and polypropylene. The surgeon may even choose to use more than one hernia mesh product to repair the damaged area.

Covidien is a subsidiary of Medtronic

Covidien is a subsidiary of Medtronic, which manufactures surgical and medical products, including surgical grade hernia plugs, patches and meshes.”U.S. medical device maker Medtronic Inc (MDT.N) said on Sunday it had agreed to buy Covidien Plc COV.N for $42.9 billion in cash and stock and move its executive base to Ireland in the latest transaction aiming for lower corporate tax rates abroad.” Reuters Parietex composite mesh, Symbotex composite mesh and Versatex monofilament mesh are Covidien products. The Parietex mesh product has been on the market since 1999 and is intended to treat advanced ventral hernias.

Parietex composite surgical mesh combines a resorbable collagen barrier with polyester, a first in the hernia mesh industry. According to Covidien, Parietex composite surgical mesh is supposed to promote integration and tissue ingrowth to minimize visceral attachments. The surgical repair of a hernia with synthetic mesh can cause severe complications.

Parietex Progrip Mesh Complications

The surgical repair of a hernia, with or without surgical hernia mesh, is known to cause complications. Some of the more common complications are hernia recurrence, perforation of surrounding organs, bleeding, obstructions, infection, pain, bowel obstruction, seromas and fistula formation. The FDA reports that hernia repair surgery with surgical mesh can cause hernia recurrence, organ adhesion, infection, pain and bowel obstruction.

Covidien indicates that the following potential complications are associated with the use of Parietex composite hernia mesh:

• Seroma
• Hematoma
• Hernia recurrence
• Infection
• Visceral adherence
• Allergic reactions

Adverse event reports

It should be noted that the above list of complications is by no means comprehensive. A number of adverse event reports related to the Parietex composite hernia mesh product have also been received by the U.S. Food and Drug Administration. The FDA’s Manufacturer and User Facility Device Experience database, or MAUDE, lists a variety of adverse health complications reported by consumers:

• Sharp pains and discomfort in the pelvis, hip or groin
• Difficulty standing for extended periods of time
• Wound leakage
• Ulcers
• Infection

ProGrip™ laparoscopic self-fixating mesh

According to medtronic, propoganda: “Designed to address key issues in laparoscopic inguinal hernia repair, ProGrip™ laparoscopic self-fixating mesh delivers tack-free fixation over the entire anatomy2, including below the inguinal ligament where traditional tacks cannot be placed.

Increases the security of the laparoscopic inguinal hernia repair†,Ω,1,2,3
Eliminates the pain associated with traditional tack fixationΩ,4,5
Is easy to use and faster than tacks†,6,7
Lowers the cost of the laparoscopic inguinal procedure by combining the functionality of mesh and fixation into one device8,9”  Medtronic

Design Defects

Originally, Parietex hernia mesh was constructed of heavy polyester material. Although the subsequent polypropylene product was stiffer and more likely to retain its form, the polyester version of Parietex hernia mesh earned a reputation for being soft and flimsy. Both the polyester and polypropylene products can cause severe complications, but many surgeons reported that it was difficult to manipulate the polyester mesh during implantation.

lightweight polyester material

Covidien added a resorbable collagen barrier to the Parietex Composite and Parietex ProGrip products in an attempt to rectify the problem. Covidien also sells a Parietex monofilament polyester mesh. Parietex monofilament surgical mesh is made of lightweight polyester material. Unfortunately, Covidien’s improved polyester surgical mesh is still plagued with complications. Other Covidien hernia mesh design defects include:

• Unsealed polyester edges on Parietex mesh
• Tearing and fraying of Covidien Hernia Mesh
• Shrinking and tearing of Parietex Composite hernia mesh
• Exposure of underlying organs to bare polyester mesh
• Contracting, pulling and stretching of Parietex ProGrip surgical mesh

Prone to contracting

The entire Parietex Polyester hernia mesh line is prone to contracting. This causes tearing and internal injury. Covidien failed to recall the Parietex hernia mesh product line. Recalling the entire product line was the only way to shield patients from severe injury. Instead, Covidien decided to continue selling its defective products in order to swell its profit margin.

No Progrip recall

Even though other surgical mesh products have been subject to recall because of severe complications and reactions, a Covidien Parietex hernia product has never been recalled. Nevertheless, severe complications such as hernia recurrence, infection, pain and adhesion have prompted many hernia patients to file a Covidien hernia mesh lawsuit. These plaintiffs claim that they suffered injury because Covidien failed to disclose known risks related to Parietex composite surgical mesh products as required under the law.

Is a Progrip Hernia Mesh Lawsuit the Answer?

Medical device manufacturers are legally required to sell only safe products. The device manufacturer must warn surgeons and consumers of any potential complications associated with their products. When a device manufacturer fails to fulfill their obligation to safeguard the health of patients, the manufacturer can be held liable for injuries inflicted by the products it sells. Progrip hernia mesh victims may be able to recover financial damages in one or more of the following areas:

• Medical expenses
• Lost wages
• Pain and suffering
• Funeral expenses

Pursuing a Progrip hernia mesh lawsuit must meet the timelines established by law. Your ability to file a claim is definitely limited. Speak with a knowledgeable Progrip hernia mesh attorney for more information and a free complimentary case evaluation. Help is available now.