Valsartan Tablets USP recall
Valsartan Tablets USP, 320 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd Roorkee 0247661 India, Marketed by: Jubilant Cardista…
Why was Valsartan Tablets USP recalled?
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: VR417062A, Exp. 09/2019; VR417063A, VR417064A, Exp. 10/2019
- Product
- Valsartan Tablets USP, 320 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd Roorkee 0247661 India, Marketed by: Jubilant Cardista…
- Recalling firm
- Jubilant Cadista Pharmaceuticals, Inc.
- Quantity
- 7,048 bottles
- Distribution
- Product was distributed throughout the United States to wholesalers and retailers.
- Recall date
- August 29, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)