Class II · ModerateRecall completed
SEMAGLUTIDE 0.5MG/ML (0.5ML VIAL) INJECTABLE SEMAGLUTIDE 1MG/ML (0.5ML VIAL) INJ
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numbert20221026@52 t20221102@11 t20221004@44 t20221116@36 t20221011@36
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 Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
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 | Pharmacy Innovations |
Show the full FDA record
| Full product label | SEMAGLUTIDE 0.5MG/ML (0.5ML VIAL) INJECTABLE SEMAGLUTIDE 1MG/ML (0.5ML VIAL) INJECTABLE SEMAGLUTIDE 2MG/ML (0.5ML VIAL) INJECTABLE SEMAGLUTIDE 4MG/ML (0.5ML VIAL) INJECTABLE SEMAGLUTIDE 5.4MG/ML (0.5ML VIAL) INJECTABLE, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA. |
| Recalling firm | Pharmacy Innovations |
| Distribution | Nationwide in the USA |
| Quantity | N/A |
| Recall initiated | 2022-12-22 |
| Report date | 2023-02-01 |
| Recall completed | 2024-07-31 |
| Recall number | D-0236-2023 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Erie PA 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.