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Product Recalls & Refunds Online / National

Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 60

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

Recall reason: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment limit of 12.5ppm.. Recalled by Breckenridge Pharmaceutical, Inc.. Distribution: U.S. Nationwide. Classification (Class II — potential health risk). Affected lots/NDC/dates: 90-count- Lot # 240721C; Exp. 02/28/2027 1000-count- Lot #230286C; Exp.02/28/2026. 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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