Semaglutide Inj recall (New Life Pharma LLC)
DrugClass IIOngoing
Summary: New Life Pharma LLC is recalling Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.. Reason: Lack of Assurance of Sterility.
What is being recalled
Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.
Why
Lack of Assurance of Sterility
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
OH
How to tell if yours is affected
Lot 241113, Exp Date 11/30/2026 & Lot 250103, Exp Date 1/31/2027
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0392-2026 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | February 26, 2026 |
| Reported | March 11, 2026 |
| Company | New Life Pharma LLC |
| Company location | Northvale, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 820 vials |
More recalls from New Life Pharma LLC · all drug recalls · recalls from February 2026