Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-007-13
Reported: May 1, 2024 Initiated: April 9, 2024 #D-0466-2024
Product Description
Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-007-13
Reason for Recall
Cross Contamination with Other Products
Details
- Recalling Firm
- Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.
- Units Affected
- 108,192/30 count bottles or 7 count blister packs
- Distribution
- USA nationwide.
- Location
- Tokushima, N/A
Frequently Asked Questions
What product was recalled? ▼
Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-007-13. Recalled by Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.. Units affected: 108,192/30 count bottles or 7 count blister packs.
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-0466-2024.
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