FDAFDA · Food and drugs·Recall number D-1550-2016
Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx only, Manufactured by: Dr. Reddy's Laboratories, Inc., 200 Somerset Corporate Blvd Floor 7, Bridgewater, NJ 08807, NDC 63739-0555-10
Published October 5, 2016 · Recall initiated: September 8, 2016
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
Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Mckesson Packaging Services
- Distributor
- Nationwide
- Lot
- Lot # 0111295, Exp 9/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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