US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 15, 2017 (10 years ago)

Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister…

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

Why it was recalled

Failed dissolution specifications - low dissolution results at S3 stage.

What was recalled

Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
5511-113-81
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0508-2017

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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