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American Medical Systems Mesh Class Action


Update: Court-Ordered Registration and Opt Out Notice Deadline: 29 October 2021

On 7 September 2021, the Federal Court of Australia ordered that Notices be sent to eligible group members in the Astora, Boston Scientific and Second Johnson & Johnson/Ethicon* class actions.

If you are a potential group member in these class actions, you will likely receive a Notice from the Federal Court in the coming weeks. These Notices contain important information regarding your ability to register to have your individual claim considered at any mediation ordered to take place this year, as well as your rights to Opt Out of the class actions if you are a group member.

In order to have your individual claim considered in these class actions, you must complete the Claimant Registration Form contained within the notice, and return it to Shine by 29 October 2021.

A copy of the Notice can be found here.

*If you have received a Johnson & Johnson / Ethicon implant listed below and suffered one or more complications after 4 July 2017, please continue reading this update. If you are a member of the First Johnson & Johnson/Ethicon Mesh Class Action, meaning you received an implant prior to 4 July 2017, no further action is required from you unless you have also had an implant included in the other class actions listed.

Alternatively, you can complete a Registration Form online at www.australianmeshclassaction.com.au.

To complete a Registration Form online, please click the ‘Register Now’ button below and fill out the form.

Register Now


About the American Medical Systems Mesh Class Action

This class action is against the manufacturers of the implants and American Medical Systems Medical Pty who supplied the implants in Australia.

The AMS implants have been used to relieve stress urinary incontinence and pelvic organ prolapse, but instead have resulted in many severe complications for Australian women. These proceedings are brought on behalf of all women who have had one of the following implants inserted and suffered complications as a result:

  • Perigee Transobturator Anterior Prolapse Repair System;
  • Apogee Vaginal Vault and Posterior Prolapse Repair System;
  • Elevate Anterior and Apical Prolapse Repair System;
  • Elevate Apical and Posterior Prolapse Repair System;
  • SPARC Sling System;
  • MONARC Subfascial Hammock System;
  • MiniArc Single-Incision Sling System;
  • MiniArc Precise Single-Incision Sling System;
  • MiniArc Pro Single-Incision Sling System;
  • RetroArc Retropubic Sling System.

If you have received an AMS implant and want to be part of the class action, register now and our class action experts will investigate a claim on your behalf.

For more information about the products involved and further details about the class action, please see our “Common Questions” section below.

The implants and complications that are covered by these proceedings are described in our pleadings accessible below.

Supporting Documents for the AMS Class Action


Our offer to you

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Obligation-free initial consultation to assess your case confidentially

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Claim assessment process where we will explain all of the options available to you

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No Win No Fee arrangement


Common Questions

The implants that we are investigating include:

  • Perigee Prolapse Repair System;
  • Apogee Vaginal Vault Prolapse Repair System;
  • Elevate Prolapse Repair System;
  • SPARC Self Fixating Sling System;
  • Monarc Subfascial Hammock;
  • MiniArc Single Incision Sling;
  • MiniArc Precise Single Incision Sling;
  • RetroArc Retropubic Sling System.
  • MiniArc Pro Single Incision Sling

The AMS mesh implants are used to treat pelvic organ prolapse and stress urinary incontinence caused by weakened or damaged pelvic floor tissue.

It will be claimed that the implants were not fit for their purpose, were not of merchantable quality and were not safe as persons are generally entitled to expect, contravening the Trade Practices Act and Competition and Consumer Act 2010 (Cth). It will be alleged that AMS were negligent.

We are aware that there are other companies who manufacture polypropylene mesh and tape such as Boston Scientific. We are not investigating these implants or polypropylene mesh used in hernia repair.

If you have a Johnson and Johnson/ Ethicon mesh or tape implant, you may also have a claim for compensation. Shine lawyers have commenced a class action on 16 October, 2012 and can inform you of your rights. Information on this class action can be found by clicking here.

Many women have suffered complications because of the faulty mesh implants, including:

  • Erosion
  • Organ perforation
  • Recurrent prolapse
  • Recurrent stress urinary incontinence
  • Vaginal scarring
  • Pain
  • Infection
  • Bleeding
  • Painful/uncomfortable intercourse
  • Urinary problems.

Mesh erosion, also known as mesh extrusion or exposure, occurs when the mesh erodes through the vaginal wall or into nearby organs.

The US Food and Drug Administration (FDA) issued an announcement on 20 October 2008 advising of the serious complications associated with surgical mesh placed through the vagina to treat pelvic organ prolapse.

On 13 July 2012 the FDA issued an update advising that the serious complications associated with transvaginal mesh for pelvic organ prolapse were not rare.

No. The products are still available on the Australian market.

You may be angry or disappointed in your doctor and feel that they should have known the mesh was defective. You may also feel that your doctor was slow to respond to the side-effects you were experiencing.

While these feelings are completely valid, legally they don’t amount to negligence on the part of your doctor.

Because of this, our legal team is investigating a claim against the manufacturers rather than the doctors who prescribed them.

You may be entitled to compensation, and if you are considered eligible for this then it will be assessed based on your injuries and whether they are ongoing.

However, you may be able to claim for:

  • Pain and suffering as well as loss of enjoyment of life
  • Past and future loss of earnings
  • Loss of earning capacity
  • Paid care and help such as nurses, gardeners, etc.
  • Past and future medical expenses
  • Out-of-pocket expenses.

The amount you will be able to claim will depend on the particular facts of your situation.

Once we have put together all of the evidence we should be able to give you a better idea of what to expect.

We work on a No Win No Fee basis and you’ll only pay our fees if you win your case at the end of the claim.

Your legal costs will be determined by the amount of work required to resolve your claim.

Currently, the firm is in the process of collecting evidence and registering the interest of women affected by these implants in participating in this potential action.

Please check the Shine website regularly for updates as to the progression of the matter.

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