Why it was recalled
Out of specification (OOS) for Spectroscopic Identification test by IR.
Product description
Aripiprazole Tablets, USP, 20 mg, Rx Only, Packaged in 500-count bottle Manufactured by: Alkem Laboratories Ltd., INDIA Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054, NDC#: 67877-434-05
Lot numbers, UPCs & expiration codes
Lot #22143120, Exp. Date: June 2024
Where it was sold
Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0539-2023
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Mar 17, 2023
- FDA report date
- Apr 26, 2023
- Quantity
- 135 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Ascend Laboratories, LLC
Original FDA data
Every field from FDA enforcement report D-0539-2023, exactly as published.
Show all FDA fields
- City
- Parsippany
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 91918
- Address
- 339 Jefferson Rd Ste 101
- Code information
- Lot #22143120, Exp. Date: June 2024
- Postal code
- 07054-3707
- Report date
- Apr 26, 2023
- Product type
- Drugs
- Recall number
- D-0539-2023
- Classification
- Class II
- Recalling firm
- Ascend Laboratories, LLC
- Product quantity
- 135 bottles
- Reason for recall
- Out of specification (OOS) for Spectroscopic Identification test by IR.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Aripiprazole Tablets, USP, 20 mg, Rx Only, Packaged in 500-count bottle Manufactured by: Alkem Laboratories Ltd., INDIA Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054, NDC#: 67877-434-05
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Mar 17, 2023
- Initial firm notification
- Letter
- Center classification date
- Apr 19, 2023