Class II · Moderate riskTerminated Initiated Mar 15, 2021 (5 years ago)
Balziva 28 Day (norethindrone and ethinyl estradiol tablets USP) 6 Blister Card…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
What was recalled
Balziva 28 Day (norethindrone and ethinyl estradiol tablets USP) 6 Blister Card Dispensers, 28 tablets each, Rx Only, Manufactured for: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-9034-58
Recalling firm
Cardinal Health Inc.
NDC code
0555-9034-58
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0579-2021
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.