US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 13, 2022 (4 years ago)

Olanzapine Orally Disintegrating Tablets, USP 10 mg, 30-count box unit dose tablets (3…

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

Why it was recalled

cGMP deviations: Temperature abuse

What was recalled

Olanzapine Orally Disintegrating Tablets, USP 10 mg, 30-count box unit dose tablets (3 blister cards each containing 10 tablets), Rx only, MFG: PAR PHARMA, NDC 49884-321-55

Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
NDC code
49884-321-55
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1042-2022

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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