US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 2, 2018 (8 years ago)

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Cross Contamination with Other Products

What 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

Recalling firm
Sandoz Inc
NDC code
16714-439-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0262-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Nitrofurantoin recalls

See all