FDAFDA · Food and drugs·Recall number D-220-2013
Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp., Eatowntown, NJ 07724 by Hikma Pharmaceuticals, Amman, Jordan, NDC 0143-9928-01
Published April 3, 2013 · Recall initiated: February 6, 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 Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- CIPROFLOXACIN
- Manufacturer
- West-ward Pharmaceutical Corp.
- Distributor
- GA, AR
- Lot
- Lot #: CB222A, Exp 06/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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