Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Out of specification (OOS) for Spectroscopic Identification test...
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 Ascend Laboratories, LLC directly.
Affected Products
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
Quantity: 135 bottles
Why Was This Recalled?
Out of specification (OOS) for Spectroscopic Identification test by IR.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ascend Laboratories, LLC
Ascend Laboratories, LLC has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report