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.
Reported: May 1, 2024 Initiated: April 9, 2024 #D-0467-2024
Product Description
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.
Reason for Recall
Cross Contamination with Other Products
Details
- Recalling Firm
- Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.
- Units Affected
- N/A
- Distribution
- USA nationwide.
- Location
- Tokushima, N/A
Frequently Asked Questions
What product 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.. Recalled by Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.. Units affected: N/A.
Why was this product recalled? ▼
Cross Contamination with Other Products
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 1, 2024. Severity: Low. Recall number: D-0467-2024.
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