US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 9, 2017 (9 years ago)

Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by…

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

Why it was recalled

Failed Tablet/Capsule Specifications; potential presence of broken tablets.

What was recalled

Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICALS IND, LTD, Jerusalem Israel, Manufactured For: TEVA PHARMACEUTICALS USA, North Wales, PA, NDC 00093-7772-05

Recalling firm
Teva Pharmaceuticals USA
NDC code
00093-7772-05
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0096-2018

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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