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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. 2024-05-01 Health moderate FDA
Health · FDA · Recall #FDA-D-0467-2024

Abilify (aripiprazole), 10 mg tablets, packaged in a) 30 count bottles (NDC 59148-008-13)… Recall

Issued May 1, 2024 · Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

In May 2024, Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. recalled the Abilify (aripiprazole), 10 mg tablets, packaged in a) 30 count bottles (NDC 59148-008-13)…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Cross Contamination with Other Products

What you should do

  1. 1 Stop using Abilify (aripiprazole), 10 mg tablets, packaged in a) 30 count bottles (NDC 59148-008-13)… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.
Category
Health
Recall date
May 1, 2024
Units affected
Not reported
Sold at
USA nationwide.
Recall number
FDA-D-0467-2024
Made in
Japan
Issuing agency
FDA

In context

Read the official FDA notice

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