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UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF WEST VIRGINIA AT CHARLESTON IN RE: ETHICON, INC., PELVIC REPAIR SYSTEM PRODUCTS LIABILITY LITIGATION THIS DOCUMENT RELATES TO ALL CASES Master File
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Who needs pelvic repair system products:

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Women who have experienced pelvic organ prolapse, a condition where the pelvic organs (such as the bladder, uterus, or rectum) protrude into the vaginal area due to weakened pelvic floor muscles.
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Women who have undergone childbirth, especially multiple pregnancies or delivered large babies, which can cause damage to the pelvic area.
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Individuals with a connective tissue disorder or conditions that weaken the pelvic floor muscles, such as Ehlers-Danlos syndrome or Marfan syndrome.
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Women with a history of pelvic surgery or injury that has led to pelvic floor dysfunction.
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It is crucial for potential users to consult with their healthcare provider to determine their specific needs and suitability for pelvic repair system products before using them. A proper diagnosis and assessment by a medical professional is essential in identifying the best course of treatment.
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Pelvic repair system products are medical devices designed to treat pelvic organ prolapse and stress urinary incontinence.
Manufacturers, importers, and distributors of pelvic repair system products are required to file with the appropriate regulatory authorities.
Pelvic repair system products should be filled out with all relevant information regarding the device, including specifications, materials used, intended use, and safety data.
The purpose of pelvic repair system products is to provide support and reinforcement to the pelvic organs to alleviate symptoms associated with pelvic organ prolapse and stress urinary incontinence.
Information such as device specifications, materials, intended use, safety data, adverse events, and any recalls or market withdrawals must be reported on pelvic repair system products.
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