Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Watson Laboratories Inc to request your refund or repair — edit it as you like.
Subject: Recall D-1400-2012 — Watson Laboratories Inc Watson Laboratories Inc recalls Loxapine Capsules USP, 10mg, 100 count bott Hello, I own a Watson Laboratories Inc recalls Loxapine Capsules USP, 10mg, 100 count bottle, Rx only, Manufactured By: Watson Laboratories Inc., Corona, CA 92880 Rx that is covered by recall D-1400-2012 from Watson Laboratories Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
