PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: November 21, 2018 Initiated: November 2, 2018 #D-0262-2019

Product Description

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

Reason for Recall

Cross Contamination with Other Products

Details

Recalling Firm
Sandoz Inc
Units Affected
23053 bottles
Distribution
Nationwide within the United States
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by Sandoz Inc. Units affected: 23053 bottles.
Why was this product recalled?
Cross Contamination with Other Products
Which agency issued this recall?
This recall was issued by the FDA Drug on November 21, 2018. Severity: Low. Recall number: D-0262-2019.