Class II · ModerateActive recall
Sermorelin
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot# SER-081726-1-10, Beyond Use Date: 10/01/2026.
Where it was soldNationwide in the USA.
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 process control
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 | Houston Rx LLC |
Show the full FDA record
| Full product label | Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032. |
| Recalling firm | Houston Rx LLC |
| Distribution | Nationwide in the USA. |
| Quantity | 7 vials |
| Recall initiated | 2026-09-25 |
| Report date | 2026-10-21 |
| Recall completed | — |
| Recall number | D-0041-2027 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Houston TX 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.