Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. recalls Abilify (aripiprazole), 10 mg tablets, packaged in a) 30 count bottles (NDC 59148-008-13) and b) 7 count blister packs…
- Recall date
- April 9, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0467-2024
- FDA classification
- Class III
- Brand / firm
- Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.
- Sold / distributed
- USA nationwide.
Why it was recalled
Cross Contamination with Other Products
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Abilify (aripiprazole), 10 mg tablets, packaged in a) 30 count bottles (NDC 59148-008-13) and b) 7 count blister packs (NDC 59148-008-95), RX only, Otsuka America Pharmaceutical, Inc.
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