Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Levetiracetam Tablets USP Recalled by McKesson Corporation dba McKesson Drug Company Due to Labeling; Wrong Barcode; error in the machine-readable barcode...
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 McKesson Corporation dba McKesson Drug Company directly.
Affected Products
Levetiracetam Tablets USP, 250 mg UD 100 Tablets (10x10) boxes, Rx Only, Distributed By: McKesson Corporation 4971 Southridge Blvd., Suite 101 Memphis, TN 38141 Manufactured by: Aurobindo Pharma Limited Hyderabad-500 090, India NDC 63739-795-10
Quantity: 210 cartons
Why Was This Recalled?
Labeling; Wrong Barcode; error in the machine-readable barcode which could result in some units being read as Naproxen Tablets 500 mg. Product is labeled correctly as Levetiracetam
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About McKesson Corporation dba McKesson Drug Company
McKesson Corporation dba McKesson Drug Company has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report