Class III · Lower riskRecall completed
Lisinopril Tablets USP
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot # FC1960; Exp.: 02/18
Where it was soldNationwide
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
Labeling: Incorrect or Missing Package Insert
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
| Distributed by / for | Sandoz Inc |
| NDC | 0185-0630-01 |
Show the full FDA record
| Full product label | Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01 |
| Recalling firm | Sandoz Inc |
| Distribution | Nationwide |
| Quantity | 3,048 bottles ( 304,800 tablets) |
| Recall initiated | 2016-05-25 |
| Report date | 2016-06-22 |
| Recall completed | 2017-04-25 |
| Recall number | D-1036-2016 |
| 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.