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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Northwest Compounders Semaglutide Injectable Recalled for Sterility Concerns

Agency Publication Date: April 13, 2026
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Summary

PAYLESS COMPOUNDERS, LLC is recalling 91 vials of Semaglutide-Glycine-Cyanocobalamin Injectable (brand name Northwest Compounders) due to a lack of assurance of sterility. Using a non-sterile injectable medication can lead to serious or life-threatening infections at the injection site or in the bloodstream. The affected products include 0.5 mL vials in 2.5 mg and 5 mg strengths, primarily distributed in Oregon.

Risk

The lack of sterility assurance means the injectable medication may contain microorganisms that could cause serious infections or other health complications if administered.

What You Should Do

  1. Check your medication vials for Northwest Compounders Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials with Lot Number 01-27-2026@14S.5.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions or to report adverse effects.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Semaglutide-Glycine-Cyanocobalamin Injectable (0.5 mL vials)by Northwest Compounders
Variants: 2.5 mg, 5 mg, 1 MG/ML
Lot Numbers:
01-27-2026@14S.5

Rx only

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98646
Status: Active
Manufacturer: PAYLESS COMPOUNDERS, LLC
Sold By: Northwest Compounders
Manufactured In: United States
Units Affected: 91
Distributed To: Oregon

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.