McKesson Corporation dba McKesson Drug Company recalls Levetiracetam Tablets USP, 250 mg UD 100 Tablets (10x10) boxes, Rx Only, Distributed By: McKesson Corporation 4971 Sout…
- Recall date
- May 26, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0630-2021
- FDA classification
- Class III
- Brand / firm
- McKesson Corporation dba McKesson Drug Company
- Sold / distributed
- Nationwide in the US
Why it was 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
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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
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