CLASS II ONGOING Drug recall · Reported 11 Mar 2026 · FDA Enforcement Report

Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial recalled

New Life Pharma is recalling Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, distributed in Ohio. The recall was initiated on 26 Feb 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 241113, Exp Date 11/30/2026 & Lot 250103, Exp Date 1/31/2027
Quantity recalled820 vials

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-0392-2026
FDA event ID
98496
Recalling firm
New Life Pharma, Northvale, NJ
Classification
Class II
Status
Ongoing
Recall initiated
26 Feb 2026
FDA classified
17 Mar 2026
Reported
11 Mar 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

26 Feb 2026Recall initiated by company
11 Mar 2026Published in enforcement report+13 days
17 Mar 2026Classified by FDA+6 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 Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.

Where it was distributed

OH

Ohio

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot 241113, Exp Date 11/30/2026 & Lot 250103, Exp Date 1/31/2027

Where was it sold?

OH

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 98496

This product is part of a recall event; the main page for the event is Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial recalled.

More recalls from New Life Pharma

All 4

Other Semaglutide Inj recalls

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISemaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial recalledNew Life PharmaSterilityOH