US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 28, 2024 (2 years ago)

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Superpotent Drug: The 3-month stability result for assay was found to be above specification limit

What was recalled

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054. Blister Pack NDC 0591-2436-45, Carton NDC 0591-2436-15

Recalling firm
Teva Pharmaceuticals USA, Inc
NDC code
0591-2436-45
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0439-2024

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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