Glover v. Bausch & Lomb, Inc., No. 20-1156 (2d Cir. 2021)
Annotate this Case
After 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, plaintiff challenged the district court's grant of 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 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.
The court issued a subsequent related opinion or order on August 8, 2022.
Some case metadata and case summaries were written with the help of AI, which can produce inaccuracies. You should read the full case before relying on it for legal research purposes.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.