Class II · ModerateActive recall
Semaglutide with B12 for Injection
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberAll lots within expiry.
Where it was soldUS Nationwide.
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 | GenoGenix LLC |
Show the full FDA record
| Full product label | Semaglutide with B12 for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. |
| Recalling firm | GenoGenix LLC |
| Distribution | US Nationwide. |
| Recall initiated | 2025-07-30 |
| Report date | 2025-10-15 |
| Recall completed | — |
| Recall number | D-0083-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Boca Raton 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.