FDAFDA · Food and drugs·Recall number D-0262-2019
Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141 Manufactured by: Sandoz Inc. Princeton, NJ 08540,NDC 16714-439-01
Published November 21, 2018 · Recall initiated: November 2, 2018
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
Cross Contamination with Other Products
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Inc
- Distributor
- Nationwide within the United States
- Lot
- Lot #: JA7319, JA 7320, JA7321, Exp. 03/2020
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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