RECALL DATABASE

Semaglutide Recall: Northwest Compounders Lot 01-27-2026@14S.5

Announced 2026-04-22 · FDA

The FDA recall concerns 91 vials of Semaglutide-Glycine-Cyanocobalamin Injectable, Rx only, from Northwest Compounders in Beaverton, OR, due to lack of assurance of sterility. The recall is associated with Lot Number 01-27-2026@14S.5 and is limited to Oregon; no corrective action is provided in the notice.

BrandPAYLESS COMPOUNDERS, LLC
ProductSemaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beaverton, OR
ReasonLack of Assurance of Sterility
Severitymoderate
Units affected91
DistributionOR
AgencyFDA

WHAT YOU SHOULD DO

  1. Do not use any recalled vials.
  2. Check your inventory for Lot 01-27-2026@14S.5 and set aside any affected product.
  3. Contact your pharmacist or Northwest Compounders for disposal or replacement instructions and stop use until advised.
  4. If you have used this product and have health concerns, contact your healthcare provider immediately.

How to identify the recalled item

Lot / date codesLot Number 01-27-2026@14S.5
Lot / date codesLot Number 01-27-2026@14S.5

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

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This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.