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Product Recalls & Refunds Online / National

Breckenridge Pharmaceutical, Inc: Duloxetine Delayed-Release Capsules, USP, 30mg

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit. Recalled by Breckenridge Pharmaceutical, Inc. Distribution: US Nationwide.. Classification (Class II — potential health risk). Affected lots/NDC/dates: 220265: Exp. Feb 2025 220088: Exp. Nov 2024 220267: Exp. Feb 2025 220256: Exp. Feb 2025 220225: Exp. Jan 2025 220269: Ex. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who purchased the recalled drug or medication. Return it to the pharmacy where you bought it for a full refund. You generally do not need the original receipt — the pharmacist can look up your purchase history.
Source Official Source ↗
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