Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. Due to Cross Contamination with Other Products

Date: April 9, 2024
Company: Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. directly.

Affected Products

Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC 59148-007-13

Quantity: 108,192/30 count bottles or 7 count blister packs

Why Was This Recalled?

Cross Contamination with Other Products

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. has 4 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report