CLASS II ONGOING Drug recall · Reported 13 Aug 2025 · FDA Enforcement Report

Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/ Inj Sol recalled

Aequita Pharmacy is recalling Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/ Inj Sol, Inject on syringe) subcutaneously, distributed in Massachusetts. The recall was initiated on 18 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Lots within expiry.
Quantity recalled190 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-0563-2025
FDA event ID
97292
Recalling firm
Aequita Pharmacy, Kirkland, WA
Classification
Class II
Status
Ongoing
Recall initiated
18 Jul 2025
FDA classified
1 Aug 2025
Reported
13 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons

Timeline

18 Jul 2025Recall initiated by company
1 Aug 2025Classified by FDA+14 days
13 Aug 2025Published in enforcement report+12 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 Processing Controls.

Product as listed by the FDA

Semaglutide +Cyanocobalamin 1.5 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.

Where it was distributed

MA

Massachusetts

Questions about this recall

Why was it recalled?

Lack of Processing Controls.

Which lots are affected?

All Lots within expiry.

Where was it sold?

MA

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.

Other products in this recall event

12 other products · FDA event 97292

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