Otsuka recalls Abilify 30mg tablets (NDC 59148-011-13) due to cross contamination risk. Affected lots: APS00423A (exp 07/31/2025) and APS00222A (exp 11/30/2024).
Cross Contamination with Other Products
Otsuka is recalling Abilify 30mg tablets that may have been contaminated with other products. This could lead to unintended medication effects if taken. Patients should check their bottle labels and contact their doctor if unsure.
Cross contamination with other products during manufacturing could introduce unintended substances into the medication. This might cause unexpected side effects or interactions with other medications.
Patients prescribed Abilify 30mg tablets by a doctor. Those with specific lot numbers are most at risk due to potential cross contamination.
Check for the lot numbers APS00423A (expiring July 31, 2025) or APS00222A (expiring November 30, 2024) on the bottle label. The product is a 30-count bottle of Abilify 30mg tablets, prescription-only.
Look for the lot numbers APS00423A (expiring July 31, 2025) or APS00222A (expiring November 30, 2024) on the bottle label.
The recall is due to potential cross contamination with other products, which could cause unintended medication effects. Consult your doctor if you have the affected lot numbers.
Check your bottle label for the lot numbers APS00423A (expiring July 31, 2025) or APS00222A (expiring November 30, 2024). Contact your doctor for guidance.
Look for the lot numbers APS00423A (expiring July 31, 2025) or APS00222A (expiring November 30, 2024) on the bottle label. The product is a 30-count bottle of Abilify 30mg tablets, prescription-only.
We’ve drafted a message you can send Otsuka to request your refund or repair — edit it as you like.
Subject: Recall D-0469-2024 — Otsuka Otsuka Hello, I own a Otsuka that is covered by recall D-0469-2024 from Otsuka. 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.
