FDAFDA · Food and drugs·Recall number D-0470-2017
Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ 08810, NDC 55150-202-00
Published February 15, 2017 · Recall initiated: December 16, 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
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PANTOPRAZOLE SODIUM
- Manufacturer
- Aurobindo Pharma USA Inc
- Distributor
- Nationwide in US
- Lot
- Lot #: CPO160028, Exp. June 2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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