Court: US Court of Appeals for the Second Circuit
Docket: 20-1156
Opinion Date: July 20, 2021
Judge: Gerard E. Lynch
Areas of Law: Personal Injury, Products Liability
After the plaintiff suffered post-operative injuries following implantation of artificial lenses during cataract surgery, she and her husband filed suit against Bausch & Lomb, the manufacturer of the lenses, as well as related entities. On appeal, the plaintiff challenged the district court’s grant of the defendants’ motion to dismiss the negligence and failure-to-warn claims and denial of the motion for leave to amend the complaint to add a claim based on wrongful marketing.
The Second Circuit reserved the decision and certified two questions to the Supreme Court of Connecticut: 1) Whether a cause of action exists under the negligence or failure-to-warn provisions of the Connecticut Product Liability Act, Conn. Gen. Stat. 52-572h, 52-572q, or elsewhere in Connecticut law, based on a manufacturer’s alleged failure to report adverse events to a regulator like the FDA following approval of the device, or to comply with a regulator’s post-approval requirements. 2) Whether the Connecticut Product Liability Act’s exclusivity provision, Conn. Gen. Stat. 52-572n, bars a claim under the Connecticut Unfair Trade Practices Act, Conn. Gen. Stat. 42-110a, et seq., based on allegations that a manufacturer deceptively and aggressively marketed and promoted a product despite knowing that it presented a substantial risk of injury.
This case law update is brought to you by Freeway Law auto accident and personal injury law attorneys. The following is not one of our cases, but it is of some significance, and we thought we should share it with our readers for informational purposes. The information above is for informational purposes only and not to be construed as legal advice.
