US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 16, 2022 (5 years ago)

Olanzapine Tablets, USP 10 mg, 30-count bottles, Rx only, Manufactured for: Macleods…

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

Why it was recalled

cGmp Deviations

What was recalled

Olanzapine Tablets, USP 10 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma USA , Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, HImachal Pradesh, India, NDC 33342-070-07.

Recalling firm
Macleods Pharma Usa Inc
NDC code
33342-070-07
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0639-2022

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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