Class II · ModerateActive recall
Semaglutide for Injection
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot#: GG021125-001, GG031125-017, 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 | Synergy Wellness, 20 mg, 10mL vial lyophilized |
Show the full FDA record
| Full product label | Semaglutide for Injection, a) 20 mg b) 20 mg/mL, 10 mL Multi-Dose Vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness, 20 mg, 10mL vial lyophilized. |
| Recalling firm | GenoGenix LLC |
| Distribution | US Nationwide. |
| Recall initiated | 2025-07-30 |
| Report date | 2025-10-15 |
| Recall completed | — |
| Recall number | D-0091-2026 |
| 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.