PlainRecalls
FDA Drug Low Class III Ongoing

Abilify (aripiprazole), 30 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-011-13

Reported: May 1, 2024 Initiated: April 9, 2024 #D-0469-2024

Product Description

Abilify (aripiprazole), 30 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-011-13

Reason for Recall

Cross Contamination with Other Products

Details

Units Affected
N/A
Distribution
USA nationwide.
Location
Tokushima, N/A

Frequently Asked Questions

What product was recalled?
Abilify (aripiprazole), 30 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-011-13. 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-0469-2024.