Otsuka recalls Abilify 5mg tablets (NDC 59148-007-13) due to cross contamination risk. Affected lots expire 01/31/2026 or 02/28/2025. Check your bottle label for lot numbers.
Cross Contamination with Other Products
Otsuka is recalling Abilify 5mg tablets that may have been contaminated with other products. This could lead to unintended medication effects if taken. People with mental health conditions using this medication should check their bottle labels.
Cross contamination with other products means the tablets might contain unintended substances. This could cause unexpected medication effects or interactions. The risk is low but requires checking the specific lot numbers.
People with prescriptions for Abilify 5mg tablets who received these specific lot numbers from Otsuka America Pharmaceutical. Those with mental health conditions using this medication are most at risk.
Check your Abilify 5mg tablets for the lot number on the bottle label. The affected lots are AKS00623A (expires 01/31/2026) or AKS00322A (expires 02/28/2025).
Look for the lot number on the bottle label to see if it matches AKS00623A (expires 01/31/2026) or AKS00322A (expires 02/28/2025).
The tablets may have been contaminated with other products, which could cause unintended medication effects.
Check your bottle label for the lot number AKS00623A (expires 01/31/2026) or AKS00322A (expires 02/28/2025).
No, but you should check your bottle label to see if it's in the recalled lots. If it is, contact your doctor.
We’ve drafted a message you can send Otsuka to request your refund or repair — edit it as you like.
Subject: Recall D-0466-2024 — Otsuka Otsuka Hello, I own a Otsuka that is covered by recall D-0466-2024 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.