870,531 bottles Clonazepam 0.5 mg & 1.0 mg tablets

[notyard]

FDA class II recall:

PRODUCT
1) Clonazepam Tablets, USP, 0.5 mg in 100 count bottles (NDC 0093-0832-01 - shipped 120 bottles per case) and 500 count bottles (NDC 0093-0832-05 - shipped 72 bottles per case), Rx Only. Recall # D-026-2010;
2) Clonazepam Tablets 1.0 mg in 100 count bottles (NDC 0093-0833-01 - shipped 144 bottles per case), 500 count bottles (NDC 0093-0833-05 - shipped 48 bottles per case) and 1000 count bottles (NDC 0093-0833-10 - shipped 36 bottles per case), Rx Only. Recall # D-027-2010
CODE
1) Lot numbers: 35200435A exp 9/2010, 35200408A exp 9/2010, 35200409A exp 9/2010, 35200436A exp 9/2010, 35200437A exp 9/2010, 35200460A exp 9/2010, 35200462A exp 9/2010, and 35200438A exp 9/2010;
2) Lot numbers: 35200199A exp 2/2010, 35200200A exp 2/2010, 35200201A exp 2/2010, 35200218A exp 2/2010, 35200219A exp 2/2010, 35200278A exp 2/2010, 35200202A exp 2/2010, 35200248A exp 2/2010, 35200220A exp 2/2010 and 35200203A exp 2/2010
RECALLING FIRM/MANUFACTURER
Recalling Firm: Teva Pharmaceuticals USA, Inc., Sellersville, PA, by letters on August 25, 2009 and August 31, 2009.
Manufacturer: Novopharm Ltd., Scarborough, Ontario, Canada. Firm initiated recall is ongoing.
REASON
Tablets may exceed specifications for weight, thickness and potency.
VOLUME OF PRODUCT IN COMMERCE
870,531 bottles
DISTRIBUTION
Nationwide