Olanzapine recall: Subpotent
Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
Why was Olanzapine recalled?
Subpotent drug
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 # KL0664, Exp 04/15
- Product
- Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
- Recalling firm
- Apotex Inc.
- Quantity
- 5,352 bottles
- Distribution
- Nationwide
- Recall date
- May 20, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)