FDAFDA · Food and drugs·Recall number D-0219-2018
Mefenamic Acid Capsules, USP, 250 mg, 30-count bottle, Rx only, Distributed by Prasco Laboratories, Mason, OH 45040, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ 07981, NDC 66993-070-30
Published January 24, 2018 · Recall initiated: May 24, 2017
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 substance: The recall was initiated due to black particles being observed while performing routine post-release stability testing on Mefenamic acid capsules
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Shionogi Inc.
- Distributor
- U.S.A. Nationwide
- Lot
- Lot#: 7H66200103G, Exp 12/19
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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