US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 20, 2023 (3 years ago)

Simvastatin 40 mg tablets, packaged in a) 30-count bottles (NDC 70518-0060-01) and b)…

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

Why it was recalled

cGMP Deviations

What was recalled

Simvastatin 40 mg tablets, packaged in a) 30-count bottles (NDC 70518-0060-01) and b) 90-count bottles (NDC 70518-0060-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701

Recalling firm
RemedyRepack Inc.
NDC code
70518-0060-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0503-2023

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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