Akorn Inc recalls Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs, R

Recalled June 26, 2019 · FDA recall D-1392-2019 · Akorn

Hazard

Labeling: Label mix-up: Product secondary carton erroneously states 40mg instead of 30 mg, primary carton is label correctly. · FDA Class III

Units

16,216 cartons

Sold at

Nationwide USA

Description

Labeling: Label mix-up: Product secondary carton erroneously states 40mg instead of 30 mg, primary carton is label correctly.

Product

Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs, Rx Only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forest, IL 60045, NDC 61748-304-13

Manufacturer(s)

Akorn Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →