US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 19, 2021 (6 years ago)

Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only…

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

Why it was recalled

Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.

What was recalled

Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-001-03

Recalling firm
Jubilant Cadista Pharmaceuticals, Inc.
NDC code
59746-001-03
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0298-2021

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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