Losartan potassium tablets USP recall
Losartan potassium tablets USP, 50 mg, 90-count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private…
Why was Losartan potassium tablets USP recalled?
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
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 #: KN1449, Exp 06/2015
- Product
- Losartan potassium tablets USP, 50 mg, 90-count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private…
- Recalling firm
- Apotex Inc.
- Quantity
- 23,076 bottles
- Distribution
- Nationwide, Hawaii and Puerto Rico
- Recall date
- July 15, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)