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ARTICLE · 26 OCTOBER 2020

Eastern District Of Kentucky: "Voluntary Recall" Doesn't Equal "Defect"

The issue of product recalls rears its head a lot in our medical device practice. Or non-recalls, to be more precise.

United StatesLitigation, Mediation & Arbitration

The issue of product recalls rears its head a lot in our medical device practice. Or non-recalls, to be more precise. In the unsavory world of plaintiff solicitation, we have seen, over and over again, that plaintiff firms and their "phone banks" recruit potential plaintiffs by telling them that devices that remain in their bodies have been recalled by the FDA when no such recall has occurred. Plaintiffs file lawsuits under this misapprehension, and no one ever tells them it's false. It is fear mongering at its most unscrupulous.

Today's case is about something different in the world of recalled products. In Christian v. Altaire Pharms., Inc., 2020 WL 6051255 (E.D. Ky. Oct. 13, 2020) the plaintiff sued the manufacturer and seller of a nighttime eye lubricant ointment, alleging that it caused her permanent eye injury.

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This article is presented for informational purposes only and is not intended to constitute legal advice.

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