Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Loxapine Capsules USP Recalled by Watson Laboratories Inc Due to Labeling: Incorrect or Missing Package Insert: An outdated...
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 Watson Laboratories Inc directly.
Affected Products
Loxapine Capsules USP, 10mg, 100 count bottle, Rx only, Manufactured By: Watson Laboratories Inc., Corona, CA 92880 Rx only. NDC # 0591-0370-01
Quantity: 106,323 bottles
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Watson Laboratories Inc
Watson Laboratories Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report