Biomet Hip Implants
This lawsuit alleges that Biomet, Inc. and related companies were negligent in designing, manufacturing, distributing and selling the Biomet M2a Magnum, M2a 38 and ReCap Femoral Resurfacing System metal-on-metal hip implants.
This class action has been certified and applies only to:
- all persons who were implanted in Canada with metal-on-metal hip implant systems known as the M2a 38, the M2a Magnum and the ReCap Femoral Resurfacing System; and
- all other persons who by reason of a personal relationship to an implant patient have standing pursuant to section 61(1) of the Family Law Act or equivalent legislation in other provinces and territories
(“Class Members” or “Class”).
If you were implanted with the Biomet M2a Magnum, the M2a 38 or the ReCap Femoral Resurfacing System, please call 1-855-595-2629 or email firstname.lastname@example.org.
If you were implanted with a different device, you are not a member of the Class in the Biomet class action and will not qualify for any recovery obtained for Class Members. This means that if you wish to pursue a legal action, you will need to contact and retain a different law firm.