Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Steril
Summary
The FDA issued a Class II for Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 by AEQUITA PHARMACY. Reason: Lack of Processing Controls..
Details
Source
Drug Recall
External ID
D-0565-2025
Action Date
2025-08-13
Status
Ongoing
Category
drug
Product Description
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.
Lot/Code Info: All Lots within expiry.
Quantity Affected: 158 vials
Reason for Recall
Lack of Processing Controls.
Distribution
MA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-18
Company
Kirkland, WA
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 55 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
AEQUITA PHARMACY has 13 FDA actions in our database, including 13 recalls.
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 (AEQUITA PHARMACY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does AEQUITA PHARMACY have FDA actions?
AEQUITA PHARMACY has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0565-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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