US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 16, 2019 (7 years ago)

Isotretinoin Capsules, USP 10 mg. Rx Only, 3 Prescription Blister Packs of 10- Capsules…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications: Tretinoin levels slightly above specification limits.

What was recalled

Isotretinoin Capsules, USP 10 mg. Rx Only, 3 Prescription Blister Packs of 10- Capsules Each (30 Capsules)-. Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC 69238-1174-3

Recalling firm
Amneal Pharmaceuticals, Inc.
NDC code
69238-1174-3
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0321-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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