Class II · ModerateActive recall
Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot: 1643397 BUD: 10/16/2023
Where it was soldNationwide in the US
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
Sub-potent Drug
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 | Revive Rx LLC dba Revive Rx Pharmacy |
| NDC | 99000-9278-64 |
Show the full FDA record
| Full product label | Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only, Compounded Drug Product By: Revive Rx, 3831 Golf Dr A, Houston, TX 77018, NDC: 99000-9278-64. |
| Recalling firm | Revive Rx LLC dba Revive Rx Pharmacy |
| Distribution | Nationwide in the US |
| Quantity | 45 Vials |
| Recall initiated | 2023-05-11 |
| Report date | 2023-05-31 |
| Recall completed | — |
| Recall number | D-0771-2023 |
| 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.