CLASS II ONGOING Drug recall · Reported 22 Apr 2026 · FDA Enforcement Report

Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg recalled

Payless Compounders is recalling Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML vials, distributed in Oregon. The recall was initiated on 6 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number [email protected]
Quantity recalled91 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-0471-2026
FDA event ID
98646
Recalling firm
Payless Compounders, Beaverton, OR
Classification
Class II
Status
Ongoing
Recall initiated
6 Mar 2026
FDA classified
13 Apr 2026
Reported
22 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

6 Mar 2026Recall initiated by company
13 Apr 2026Classified by FDA+38 days
22 Apr 2026Published 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-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beaverton, OR

Where it was distributed

OR

Oregon

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot Number [email protected]

Where was it sold?

OR

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.