Filshie Clip Migration Lawsuit Alleges Wrongdoing By Manufacturer, Distributor, And Others: A recently filed Filshie clip migration lawsuit in Connecticut alleges on behalf of eleven women plaintiffs that one or more of the defendants (COOPERSURGICAL, INC., COOPER COMPANIES, INC., FEMCARE, LTD. – UK SUBSIDIARY OF UTAH MEDICAL PRODUCTS, INC., and UTAH MEDICAL PRODUCTS, INC.) caused them injuries:

(a) In that they placed onto the market and into the stream of commerce a product that was defective and unreasonably dangerous;
(b) In that they placed onto the market and into the stream of commerce a product that was defective and unreasonably dangerous in reckless disregard for the safety of product consumers;
(c) In that they breached an implied warranty of merchantability as said “Filshie Clips” was not of merchantable quality nor fit for its intended purpose;
(d) In that they breached its implied warranty that said “Filshie Clips” was safe and effective for its intended use;
(e) In that they failed to properly test the “Filshie Clips” to determine whether or not the product was safe for its intended use;

(f) In that they misrepresented to the plaintiff, the plaintiff’s healthcare providers and/or the general health care community that said “Filshie Clips” was safe for its intended use;
(g) In that they failed to provide adequate instructions, guidelines, and safety precautions, to those persons to whom it was reasonably foreseeable would recommend, use, implant and remove the “Filshie Clips”;
(h) In that they failed to use reasonable and prudent care in the design, research, manufacture, and development of “Filshie Clips” so as to avoid the risk of serious harm associated with the use of the “Filshie Clips”;

(i) In that they failed to provide adequate warnings and/or instructions to the plaintiff, the plaintiff’s healthcare providers and/or the general health care community about “Filshie Clip’s” substantially dangerous condition or about facts making the product likely to be dangerous, including pre-and post-sale;
(j) In that they failed to warn and instruct the Plaintiff, the plaintiff’s healthcare providers and/or the general health care community about the inadequate research and testing of the Filshie Clips, and the complete lack of a safe, effective procedure for preventing migration;
(k) In that the “Filshie Clips” was defectively designed for its intended purpose;
(l) In that they represented that “Filshie Clips” were safe for their intended use when in fact, the defendant knew and should have known the product was not safe for its intended purpose;
(m) In that they failed to establish an adequate quality assurance program used in the manufacturing of the “Filshie Clips”;
(n) In that they failed to adequately and correctly report safety information related to the “Filshie Clip” product resulting in inadequate warnings;
(o) In that they failed to provide adequate and continuous warnings about the inherent danger of migration with “Filshie Clips” after they had been placed on the fallopian tubes;
(p) In that they failed to manufacture the “Filshie Clips” in conformity with the manufacturer’s design or in conformity with the approved design that the defendants had submitted to the FDA.

WE ARE CURRENTLY INVESTIGATING FILSHIE CLIP MIGRATION CLAIMS THROUGHOUT THE UNITED STATES.

If you or a loved one suffered injury or other harm from Filshie clip migration, or other Filshie clip issues, in the United States, you should promptly find a lawyer who may investigate your Filshie clip claim for you and represent you or your loved one in a Filshie clip case, if appropriate.

Visit our website or call us toll-free in the United States at 800-295-3959 to find Filshie clip attorneys who may assist you with your Filshie clip claim.

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