Legal Question in Product Liability in Illinois
Complications from FDA approved medical device
Physician inserted medical device which is FDA approved. Design of device caused severe complications requiring 2 surgeries. American Society of Ophthalmic Plastic & Reconstruction Surgeons found device capable of causing irreversible obstruction. Number of medical specialists describe other personal experiences where this device has caused poblems. Would this be grounds for class action lawsuit? What would be the cost to me to institute such action and how would I contact someone about it? The company manufactoring the device is located in the state of Washington.
3 Answers from Attorneys
Re: Complications from FDA approved medical device
In order to seriously evaluate a potential class action concerning a defective product our office would need to meet with you and review the materials extensively. A short answer to your questions would not be feasible.
Re: Complications from FDA approved medical device
A class action lawsuit has a number of prerequisites, among them: (i) numerousity [there must be a relatively large number of class members]; (ii) typicality [the claims of the representative plaintiff must be typical of those of the absent class members]; (iii) commonality [there must be common issues of law or fact among the class members]; and (iv) adequacy of representation [the representative plaintiff and his/her counsel must adequitly represent the class members' interests]. Thus, individual issues must not predominate over common class issues.
That said, medical products liability cases can provide the basis for legitimate class actions, depending upon the particular facts -- which typically takes considerable investigation by plaintiff's counsel.
Most of the time, the attorney advances the costs in the case, to be reimbursed upon successful prosecution or settlement of the case.
-- Kenneth J. Ashman; Ashman Law Offices, LLC; [email protected]
Re: Complications from FDA approved medical device
You must prove that the product is UNREA-
ONABLY dangerous in that it contained a de-
fect in design, manufacture or a fialure to
warn. This MAY be a design defect; more
facts are warranted here before an answer
can be given. FDA approval per se is no defense. There is a 2 year
statute of limitations.