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Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol recall

FDA recall D-0565-2025 · initiated Jul 18, 2025

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Aug 13, 2025How we research

AEQUITA PHARMACY recalled Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol in Jul 2025 — an FDA Class II recall (D-0565-2025) because Lack of Processing Controls.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Lack of Processing Controls.

The manufacturing process itself

The FDA found the process itself out of compliance, usually before any defective product was identified.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

All Lots within expiry.

Quantity recalled: 158 vials

Details

Product
Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
Recalling company
AEQUITA PHARMACY
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
MA
Initiated
Jul 18, 2025
FDA report date
Aug 13, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol recalled?
AEQUITA PHARMACY recalled Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol in Jul 2025 — an FDA Class II recall (D-0565-2025) because Lack of Processing Controls. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol recalled?
Per the FDA enforcement record, the reason for recall D-0565-2025 was: Lack of Processing Controls.
Is a recalled Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol are affected?
Distributed: MA. The recall covers these lots — All Lots within expiry.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0565-2025.

Source: openFDA Drug Enforcement record D-0565-2025

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