RecallHawk
Class II Recall

Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beav

PAYLESS COMPOUNDERS, LLC

Summary

The FDA issued a Class II for Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL via by PAYLESS COMPOUNDERS, LLC. Reason: Lack of Assurance of Sterility.

Details

Source

Drug Recall

External ID

D-0471-2026

Action Date

2026-04-22

Status

Ongoing

Category

drug

Product Description

Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beaverton, OR

Lot/Code Info: Lot Number 01-27-2026@14S.5

Quantity Affected: 91 vials

Reason for Recall

Lack of Assurance of Sterility

Distribution

OR

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-06

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 94 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (PAYLESS COMPOUNDERS, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does PAYLESS COMPOUNDERS, LLC have FDA actions?

This is the only FDA action we have on record for PAYLESS COMPOUNDERS, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0471-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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