FDAFDA · Food and drugs·Recall number D-1702-2012
Levetiracetam Tablets, USP 500 mg, 500 count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-5615-05
Published October 3, 2012 · Recall initiated: July 27, 2012
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
Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LEVETIRACETAM
- Manufacturer
- Mylan Pharmaceuticals Inc.
- Distributor
- The product was distributed to KY.
- Lot
- Lot ZLMM12063, Exp March 2014
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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