Class II · ModerateActive recall
Lisinopril 20 mg/ml Injection
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberA5028 Exp 6/2/13
Where it was soldNationwide and PR
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
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
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
| Distributed by / for | Lowlite Investments, Inc. D/B/A Olympia Pharmacy |
Show the full FDA record
| Full product label | Lisinopril 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL |
| Recalling firm | Lowlite Investments, Inc. D/B/A Olympia Pharmacy |
| Distribution | Nationwide and PR |
| Quantity | 1 |
| Recall initiated | 2013-05-29 |
| Report date | 2013-07-17 |
| Recall completed | — |
| Recall number | D-749-2013 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Orlando FL 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.