FDAFDA · Food and drugs·Recall number D-147-2013
Lansoprazole Delayed-release Capsules, USP, 30 mg, 500-count capsules per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., Made in India, NDC 0378-8030-05.
Published February 13, 2013 · Recall initiated: January 30, 2013
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
Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg delayed-release capsules may contain topiramate 100 mg tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LANSOPRAZOLE
- Manufacturer
- Mylan Pharmaceuticals Inc.
- Distributor
- Nationwide
- UPC
- 0303788030932
- Lot
- Lot #: 1110829, Exp 05/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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