Class III · Lower riskRecall completed
Nitrofurantoin Capsules
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot #: JA7319, JA 7320, JA7321, Exp. 03/2020
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Cross Contamination with Other Products
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made bySandoz Inc. Princeton, NJ 08540,NDC 16714-439-01
| Distributed by / for | Northstar Rx LLC Memphis, TN 38141 |
| NDC | 16714-439-01 |
Show the full FDA record
| Full product label | 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 |
| Distribution | Nationwide within the United States |
| Quantity | 23053 bottles |
| Recall initiated | 2018-11-02 |
| Report date | 2018-11-21 |
| Recall completed | 2020-10-02 |
| Recall number | D-0262-2019 |
| Classification | Class III |
| FDA status | Terminated |
| Origin on file | Princeton NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.