SEMAGLUTIDE 10mg/4mL (2.5mg/mL) recall
FDA recall D-0653-2024 · initiated Aug 22, 2024
ProRx LLC recalled SEMAGLUTIDE 10mg/4mL (2.5mg/mL) in Aug 2024 — an FDA Class II recall (D-0653-2024) because Lack of Assurance of Sterility.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
Lack of Assurance of Sterility
Sterility could not be assured
The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 1,960 vials
Details
- Product
- SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
- Recalling company
- ProRx LLC
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Nationwide in the USA
- Initiated
- Aug 22, 2024
- FDA report date
- Sep 11, 2024
Frequently asked
- Was SEMAGLUTIDE 10mg/4mL (2.5mg/mL) recalled?
- ProRx LLC recalled SEMAGLUTIDE 10mg/4mL (2.5mg/mL) in Aug 2024 — an FDA Class II recall (D-0653-2024) because Lack of Assurance of Sterility. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was SEMAGLUTIDE 10mg/4mL (2.5mg/mL) recalled?
- Per the FDA enforcement record, the reason for recall D-0653-2024 was: Lack of Assurance of Sterility
- Is a recalled SEMAGLUTIDE 10mg/4mL (2.5mg/mL) dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of SEMAGLUTIDE 10mg/4mL (2.5mg/mL) are affected?
- Distributed: Nationwide in the USA. The recall covers these lots — ProRx061424, BUD 12/13/2024. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0653-2024.