CLASS II ONGOING Drug recall · Reported 5 Nov 2025 · FDA Enforcement Report
Semaglutide Injection, 5 mg/ 5 mg/mL) Multidose Vial recalled by ProRx
ProRx is recalling Semaglutide Injection, 5 mg/ 5 mg/mL) Multidose Vial, For Subcutaneous Use, distributed in Texas, Utah. The recall was initiated on 15 Oct 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0119-2026
- FDA event ID
- 97808
- Recalling firm
- ProRx, Exton, PA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 15 Oct 2025
- FDA classified
- 27 Oct 2025
- Reported
- 5 Nov 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Diabetes Medication
Timeline
| 15 Oct 2025 | Recall initiated by company | |
| 27 Oct 2025 | Classified by FDA | +12 days |
| 5 Nov 2025 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Semaglutide Injection, 5 mg/2 mL (2.5 mg/mL), 2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-02
Where it was distributed
TX and UT
Questions about this recall
Is Semaglutide Injection, 5 mg/ 5 mg/mL) Multidose Vial, For Subcutaneous Use recalled?
Yes. ProRx recalled Semaglutide Injection, 5 mg/ 5 mg/mL) Multidose Vial, For Subcutaneous Use on 15 Oct 2025. The recall is Class II and its status is Ongoing. Recall number D-0119-2026.
Why was it recalled?
Lack of Assurance of Sterility
Which lots are affected?
Lot PRORX052125-4
Where was it sold?
TX and UT
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from ProRx
All 14| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Semaglutide Injection 5 mg/mL) Multidose Vial, For Subcutaneous Use recalled | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Tirzepatide Injection, 27 mg/ (9 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 8mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 5mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 6mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
Other Semaglutide recalls
All 8| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Semaglutide Injection 5 mg/mL) Multidose Vial, For Subcutaneous Use recalled | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 8mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 5mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 6mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 10 mg/ 5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |