FDAFDA · Food and drugs·Recall number D-0490-2023
Aripiprazole 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2921-03
Published April 12, 2023 · Recall initiated: March 20, 2023
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP Deviations
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- RemedyRepack Inc.
- Distributor
- RemedyRepack distributed product to consignees nationwide within the United States
- Lot
- Lot #: J0620431-052322, Exp. Date 05/31/23
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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