Sandoz Inc recalls Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100
See all recalls from Sandoz Inc →Recalled Product
Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, packaged in a) 100-capsule bottles (NDC 0185-0122-01); and b) 1000-capsule bottles, (NDC 0185-0122-10); Rx Only, Distributed by Sandoz Inc. Princeton, NJ 08540
Hazard / Issue
Cross Contamination with Other Products
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots: a) JB4952, JA7322 Exp. 03/2020; b) JA7324, Exp.03/2020
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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