US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 17, 2012 (14 years ago)

Loxapine Capsules USP, 50mg, 100 count bottle, Rx only Manufactured By: Watson…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

What was recalled

Loxapine Capsules USP, 50mg, 100 count bottle, Rx only Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 0591-0372-01

Recalling firm
Watson Laboratories Inc
NDC code
0591-0372-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1402-2012

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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