Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due to Subpotent Drug: Out of specification (OOS) results at...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Apotex Corp. directly.
Affected Products
Olanzapine Orally Disintegrating Tablets 5 mg, 30-count Bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada M9L1T9, Manufactured for Apotex Corp., Weston, Florida 33326, NDC # 60505-3275-03
Quantity: 5,397 bottles
Why Was This Recalled?
Subpotent Drug: Out of specification (OOS) results at the 9 month temperature point.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Apotex Corp.
Apotex Corp. has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report