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RemedyRepack Inc.: Duloxetine Delayed-Release Capsules, 60 mg, a) 30 count

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 recommended interim limit.. Recalled by RemedyRepack Inc.. Distribution: Nationwide in the US. Classification (Class II — potential health risk). Affected lots/NDC/dates: a) NDC 70518-0937-04, Lot # J0786744-061724, Exp. 06/30/2025 b) NDC 70518-0937-03, Lot # B3002625-060524, Exp. 10/31/202. 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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