Posts Tagged ‘ Hernia Mesh ’

Surgical Mesh Complications Tear Lives Apart

Mar 25th, 2013 | By
Surgical Mesh Complications Tear Lives Apart

March 25, 2013~ First Coast News Jacksonville has just aired the latest mesh complication story at its Gannett station. See the story here. “The pain was severe enough that I couldn’t stay still on the bed.”  “It just became unbearable.  I went into seclusion from this.“ These are some of the comments from the four
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Some Thoughts on Mesh: Product Design & Development

Mar 6th, 2013 | By
Some Thoughts on Mesh: Product Design & Development

~March 1, 2013 I helped Adam Slater as an expert with what became Gross v Ethicon from early in 2009. My job was to help Mr. Slater make sure Ethicon had produced all its relevant documents. I have the qualifications to do that because I am a veteran researcher and have run product development for
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Why We Are Here ~ To Put a Face on Adverse Events

Jan 31st, 2013 | By
Why We Are Here ~ To Put a Face on Adverse Events

January 31, 2013 ~ Quite simply put the reason we are here at Mesh Medical Device News Desk (MDND) is to calculate the human toll of complications from the unregulated world of medical devices. Most Americans do not understand that the vast majority of medical devices 75-90% approved in the U.S. bypass any safety and
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Hernia Mesh Complications- Is the FDA Watching? Part II

Nov 28th, 2012 | By
Hernia Mesh Complications- Is the FDA Watching?  Part II

November 28, 2012 ~ Continuation from Part I, According to hernia mesh removal surgeon, Dr. Kevin Petersen, in a certain percentage of patients, the body will detect hernia mesh as a foreign material and will reject it. Symptoms may include scar tissue that leads to chronic pain and causes mesh to shrink and shrivel up,
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Hernia Mesh Complications – Is the FDA Watching? Part I

Nov 28th, 2012 | By
Hernia Mesh Complications – Is the FDA Watching? Part I

November 28, 2012 ~ The U.S. Food and Drug Administration (FDA) has been updating pages on mesh used for hernia repair. Unlike transvaginal mesh, also made of plastic polypropylene, there is no Health Notification or Safety Warning on hernia mesh. That means there are no active lawsuits involving hernia mesh, but injuries are coming into
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Dollars and Sense? Saving Money on Hernia Mesh

Sep 17th, 2012 | By
Dollars and Sense? Saving Money on Hernia Mesh

  “Application of Evidence-Based Value Analysis: Standardization of Surgical Mesh Products” In this White Paper, Winifred Hayes, a medical efficiency analyst, known as, “Your Outsourced Research Partner,” tells hospitals how to save money buying hernia mesh by being more efficient. Problem: In the case of hernia mesh, hospitals buy mesh from a limited number of
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Consumer Reports: Dangerous Medical Devices

Apr 2nd, 2012 | By
Consumer Reports: Dangerous Medical Devices

April 1, 2012 ~ The May issue of Consumer Reports (here)  features an investigation into synthetic mesh and artificial hips – medical devices that escape rigorous testing to assure safety. Tens of millions of Americans are living with medical devices and whether a defibrillator, artificial hip or surgical mesh, – 90 percent of those devices
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Sick of Suffering in Silence

Mar 19th, 2012 | By

MARCH 19, 2012 ~ By Jane Akre    A story before I tell this story.  I was commissioned to write a 2,100 word piece for the Chicago-based magazine “In These Times.”  I had pitched the long-time editor and he said they were very interested. Great I thought. The money wasn’t much but the exposure for an
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Hernia Repair: Secrets Patients Should Know

Mar 1st, 2012 | By
Hernia Repair: Secrets Patients Should Know

The Wall Street Journal’s Laura Landro writes about hernia repair and the secret patients should understand before undergoing the operation. The secret appears to be that hernia repair, one of the most common surgeries, carries a high risk of chronic pain after surgery – 30% of patients have restricted movement and chronic pain that can
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Hernia Mesh Injured Patient Jim Shull Testifies on FDA’s Lax Oversite of Medical Devices

Feb 16th, 2012 | By
Hernia Mesh Injured Patient Jim Shull Testifies on FDA’s Lax Oversite of Medical Devices

February 15, 2012 ~ Testimony of James Shull U.S House Committee on Energy and Commerce/Subcommittee on Health My name is Jim Shull and I am from Browns Mills, New Jersey. I would like to thank you for allowing me the opportunity to speak here today. My story goes back to 2005 when I was told
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We hope you find this a helpful resource. National News Editor, Jane Akre, began MDND with the hope of providing the latest news, information and perspective from the regulatory, industry and patient point of view, something that goes under-reported in much of the coverage of medical devices. The public is just now becoming aware that many devices do not undergo the same scrutiny as prescription drugs and are instead grandfathered in under an FDA loophole that has gone largely unchanged since the 1970s. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.