US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 7, 2018 (8 years ago)

Absorica (Isotretinoin) Capsules 30 mg USP, 30 capsules (3x10 Prescription Packs) Rx…

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

Why it was recalled

Subpotent Drug: Isotretinoin content results were lower than the specification limit obtained during routing product monitoring.

What was recalled

Absorica (Isotretinoin) Capsules 30 mg USP, 30 capsules (3x10 Prescription Packs) Rx only, Manufactured by: Galephar Pharmaceutical Research Inc. Humacao, PR 00792, Distributed by: Sun Pharmaceutical Industries Inc. Cranbury, NJ 08512, UPC 310631117313, NDC 10631-117-31 (carton) NDC10631-117-69 (prescription pack)

Recalling firm
Sun Pharmaceutical Industries, Inc.
NDC code
10631-117-31
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1207-2019

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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