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Amerisource Health Services LLC: Duloxetine Delayed-Release Capsules, USP, 30 mg

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 the recommended interim limit. Recalled by Amerisource Health Services LLC. Distribution: PA, OH, PR. Classification (Class II — potential health risk). Affected lots/NDC/dates: a) 30 count; Lot, expiry: DT3023019B, DT3023020A, exp 01/31/2025 b) 1000 count; Lot, expiry: DTB23098A, exp 08/31/2025. 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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