D-0521-2016 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- December 23, 2015
- Initiation Date
- October 20, 2015
- Termination Date
- November 1, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3536 bottles
Product Description
Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg, 90-count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICAL INDUSTRIES LTD Jerusalem, 971010 Israel, Manufactured for: TEVA PHARMACEUTICAL INDUSTRIES USA Sellersville, PA 18960. NDC 0093-8238-98
Reason for Recall
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Distribution Pattern
Nationwide
Code Information
Lot #: 24I030, Exp 5/2017