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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-0466-2024

Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka… 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), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka…, 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), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka… 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-0466-2024
Made in
Japan
Issuing agency
FDA

In context

Read the official FDA notice

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