Class II · ModerateActive recall
Semaglutide Inj.
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot 240903, exp 9/30/2026
Where it was soldOH
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
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 | New Life Pharma LLC |
| NDC | 84223-001-06 |
Show the full FDA record
| Full product label | Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-06 |
| Recalling firm | New Life Pharma LLC |
| Distribution | OH |
| Quantity | 2 vials |
| Recall initiated | 2026-02-26 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0393-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Northvale 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.