Losartan Potassium and Hydrochlorothiazide Tablets recall
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista…
Why was Losartan Potassium and Hydrochlorothiazide Tablets recalled?
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
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 #14P0292, Exp 04/2016
- Product
- Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista…
- Recalling firm
- Jubilant Cadista Pharmaceuticals Inc.
- Quantity
- 9,358 bottles
- Distribution
- Nationwide and Puerto Rico
- Recall date
- August 6, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)