Tag: Degrade

  • Polymers Expert Not Allowed to Opine on Content of Internal Documents

    Polymers Expert Not Allowed to Opine on Content of Internal Documents

    In December 2020, Diana Dyer “was surgically implanted with an Aris™ Trans-Obturator Sling System (hereinafter the ‘Aris’), a pelvic mesh product and medical device designed, manufactured, and marketed by Defendants,” which “was intended to treat pelvic organ prolapse and stress urinary incontinence.”

    Dyer claimed that she “has suffered, and continues to suffer, debilitating injuries” “as a result of being surgically implanted with Defendants’ unreasonably dangerous defective pelvic mesh device.”

    Dyer retained as an expert Dr. Jimmy W. Mays, a “Professor Emeritus in the Department of Chemistry at the University of Tennessee.” Mays opined that the Aris is not suitable to serve as a permanent implant.

    Coloplast sought to exclude the opinions of Mays.

    Polymers Expert Witness

    Jimmy Wayne Mays has a Ph.D. in polymer science and has worked extensively in the area of polymeric biomaterials.

    Want to know more about the challenges Jimmy Mays has faced? Get the full details with our Challenge Study report.

    Discussion by the Court

    A. Oxidative Degradation Opinions

    Mays opined that polypropylene mesh undergoes oxidative degradation in the human body, which causes the mechanical properties of the mesh to break down.

    1. Relevance and Helpfulness to Jury

    Coloplast argued that Mays’ opinions are “irrelevant and unhelpful because there is no evidence that [Dyer’s] Aris implant degraded or that any purported degradation caused her alleged injuries.”

    Dyer asserted that there is evidence in the record that the Aris’ mesh “was defective and that safer alternatives would have mitigated the complications of the ‘excessive and unpredictable’ foreign body response experienced by Dyer.” The Court agreed with Dyer and found Mays’ testimony relevant and helpful to the jury.

    2. Reliability

    Coloplast argued that Mays lacked a reliable basis to opine that Coloplast’s polypropylene mesh implants degrade in the body. Mays cited many scientific studies to support his opinion that the addition of antioxidants may delay but cannot prevent the oxidative degradation of polypropylene mesh.

    Coloplast has not demonstrated that there is too great an analytical gap between the studies Mays cited and his opinion regarding the Aris’ polypropylene mesh.

    B. Clinical Complications

    Coloplast argued that Mays “lacks the necessary qualifications to offer opinions concerning potential clinical complications resulting from the purported degradation because he is not a medical doctor and has no medical training.” In response, Dyer represented that Mays will not opine on the medical complications associated with polypropylene mesh.

    C. Reduction of Mechanical Properties

    Mays stated that the degradation of polypropylene in vivo is “accompanied by a decrease in mechanical properties (embrittlement, loss of mass, decreased melting temperature, reduced compliance) of the polypropylene.”

    Coloplast noted that Mays admittedly “is not qualified to quantify the degree of stiffness purportedly resulting from oxidative degradation in vivo or the degree of stiffness necessary to produce clinical symptoms in a patient, and he is unaware of any scientific literature attempting to do so.”

    Dyer represented that Mays will not offer opinions regarding clinical complications associated with polypropylene mesh. However, Mays, an expert in polymer science and biomaterials, cited multiple scientific articles in support of his opinions regarding the reduction of the mesh’s mechanical properties. The Court found that Mays’ opinions on this issue are reliable.

    D. Toxicology Opinions

    Coloplast argued that Mays “is unqualified to opine on the alleged toxicity or irritability of polypropylene resin or antioxidants.”

    In response, Dyer represented that “Mays will not opine as to the toxicity of polypropylene resin or antioxidants.” Accordingly, the issues of whether Mays is qualified to offer opinions on toxicity and whether his opinions are reliable and helpful to the jury are moot.

    However, Dyer did not address the issue of whether Mays is qualified to testify as to the alleged irritability of polypropylene resin or antioxidants. Accordingly, the Court treats this portion of the motion as unopposed.

    E. Safer Alternatives

    Coloplast argued that Mays “lacks both the qualifications and the necessary data to opine that polyethylene, poly(vinylidene fluoride) (PVDF), and P4HB meshes” are safer alternatives to polypropylene mesh.

    In response, Dyer represented that Mays will not opine as to whether PVDF or P4HB is “safer” than polypropylene mesh.

    Accordingly, Coloplast’s argument regarding PVDF and P4HB mesh is moot. As Dyer did not address Coloplast’s contention that Mays is not qualified to opine that polyethylene mesh is a safer alternative to polypropylene mesh, the Court treated this portion of the motion as unopposed.

    The Court granted the motion to the extent of excluding Mays’ opinion that polyethylene mesh is a safer alternative to polypropylene mesh.

    F. Legal Conclusions, Contents of Internal Documents, and Opinions on Coloplast’s State of Mind and Conduct

    Finally, Coloplast asked the Court to exclude Mays’ legal conclusions, summaries of internal documents, and opinions on Coloplast’s state of mind or corporate conduct.

    The Court denied the motion as moot to the extent Coloplast sought to preclude Mays from offering legal conclusions or opining on Coloplast’s state of mind or corporate conduct. Mays is not precluded from offering testimony that uses terms that do not have a separate, distinct, and specialized meaning in the law.

    The Court granted the motion to the extent Coloplast asked the Court to “preclude Mays from testifying as to the content of Coloplast’s internal documents.” However, Mays “may testify as to a review of internal corporate documents solely for the purpose of explaining the basis for his or her opinions — assuming the opinions are otherwise admissible.”

    Held

    The Court granted in part and denied in part Defendant Coloplast Corp.’s motion to exclude the testimony of Jimmy Mays, Ph.D.

    Key Takeaway

    Simply parroting documents or other testimony does nothing to assist the trier of fact. Mays also may not summarize Coloplast’s internal documents.

    Please refer to the blog previously published about this case:

    Gynecology Expert Not Allowed to Opine on Corporate Intent

    Case Details:

    Case Caption: Dyer V. Coloplast Corp.
    Docket Number: 8:24cv2867
    Court Name: United States District Court, Florida Middle
    Order Date: July 02, 2026
  • Obstetrics and Gynecology Expert’s Testimony on Mesh Porosity and Stiffness Admitted

    Obstetrics and Gynecology Expert’s Testimony on Mesh Porosity and Stiffness Admitted

    Connie Thacker is one of tens of thousands of individuals who have filed suit against Ethicon for injuries after treatment with Ethicon’s pelvic mesh devices. 

    Thacker filed a motion asking the Court to preclude defense expert Dr. Salil S. Khandwala from offering testimony on certain subjects. 

    Obstetrics and Gynecology Expert Witness

    Dr. Salil Siddhartha Khandwala is board-certified in obstetrics and gynecology with a subspecialty board certification in female pelvic medicine and reconstructive surgery. He has been in the practice treating women’s health issues since 2000.

    He taught as an Assistant Professor in the Division of Urogynecology and Pelvic Reconstruction Surgery department at the University of Maryland from 1998-2002.

    Want to know more about the challenges Salil S. Khandwala has faced? Get the full details with our Challenge Study report

    Discussion by the Court

    Khandwala’s testimony regarding degradation and contraction in the Ethicon mesh devices

    Khandwala was expected to testify that Ethicon’s pelvic mesh devices do not degrade or contract. Thacker argued that this testimony should be excluded because it is unreliable. Thacker contended that Khandwala’s opinions are based on (1) his statement that he “does not believe,” in those issues with respect to Ethicon’s mesh devices; and (2) a flawed methodology.

    However, Khandwala stated that his opinions on these subjects are based on his review of several studies and his own clinical experience using similar mesh devices. He also made several citations to scientific literature.

    For example, with respect to his opinion on degradation, Khandwala stated that “I have never seen [degradation] in my personal experience using this sling in over 300 cases spanning a period of 10 years and recent published scientific literature has found that Prolene mesh in fact does not degrade [citation omitted].”

    The Court found Khandwala’s opinions—that Ethicon’s pelvic mesh devices did not degrade or contract—to be reliable.

    Khandwala’s testimony regarding mesh porosity and stiffness

    Thacker suggested that Khandwala’s opinions on porosity and stiffness are unreliable because he “has never published on the porosity of mesh and has never personally examined the pore size of any of the Ethicon meshes absent observations with the naked eye.” Thacker argued that such gross examinations, on their own, are insufficient to render Khandwala’s opinions on porosity and stiffness reliable.

    The Court held that Khandwala’s testimony, however, is not solely based on the occasional examination of Ethicon’s products. Rather, the portion of his report that Thacker challenges demonstrated that Khandwala’s testimony on this subject is based on his knowledge relating to the conditions of Ethicon’s mesh products in cases where they are correctly implanted.

    And Khandwala’s knowledge on that subject was derived from both clinical and scholarly review. In fact, his expert report is replete with references to not only his own clinical experience as the basis for his knowledge relating to the conditions of Ethicon’s mesh products after implantation, but it also included numerous references to his review of relevant articles, studies, and other materials.

    Held

    The Court denied the Plaintiff’s motion to exclude the testimony of defense expert Dr. Salil S. Khandwala, M.D. 

    Key Takeaway:

    Khandwala’s opinions regarding degradation and contraction did not rest on unsupported speculation or a flawed methodology. Basically, he stated that his opinions on these subjects are based on his review of several studies and his own clinical experience using similar mesh devices.

    As a result, the Court broke no new ground in finding that Khandwala’s testimony was supported by appropriate validation and rested on a sufficient methodology.

    Case Details:

    Case Caption: Thacker V. Ethicon, Inc. Et Al
    Docket Number: 5:20cv50
    Court Name: United States District Court, Kentucky Eastern
    Order Date: July 01, 2025