RecallDepth
Class II Terminated

Zeosa (norethindrone and ethinyl estradiol tablets USP, (chewable), 0.4 mg/0.035 mg, and ferrous fumarate tablets USP, (chewable) 75 mg), 3 Blister Cards, 28 Tablets Each, Rx only, TEVA Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-2090-28 and 0093-2090-58, cartons containing three (3) individual blister packs

This recall has been terminated (originally issued July 4, 2012).

Company
Teva Pharmaceuticals Usa, Inc.
Recall Initiated
May 2, 2012
Posted
July 4, 2012
Recall Number
D-1397-2012
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
100,761 cartons
Firm Location
Sellersville, PA, United States
Official Source
View on FDA website ↗

Reason for Recall

Impurities/Degradation: This recall is being carried out due to the potential for some lots not meeting impurity specifications.

Distribution

Nationwide

Lot / Code Info

Lot #'s 33800226A, Exp 7/2012; 33800333A, Exp 10/2012; 33800870A, Exp 10/2012; 33802533A, Exp 4/2013; and 33802720A, Exp 8/2013

More recalls by Teva Pharmaceuticals Usa, Inc.

View all recalls by this company →

Other recent Class II Drug recalls