CLASS II Drug recall · Reported 18 Jan 2023 · FDA Enforcement Report

Methylcobalamin Injection Solution, 5mg/ml recalled

Northern VA Compounders P is recalling Methylcobalamin Injection Solution, 5mg/ml, distributed nationwide in the US. The recall was initiated on 30 Dec 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 11292022@16, Exp 1/13/2023
Quantity recalled2 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-0119-2023
FDA event ID
91443
Recalling firm
Northern VA Compounders P, Sterling, VA
Classification
Class II
Status
Terminated
Recall initiated
30 Dec 2022
FDA classified
12 Jan 2023
Reported
18 Jan 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Sterility

Timeline

30 Dec 2022Recall initiated by company
12 Jan 2023Classified by FDA+13 days
18 Jan 2023Published in enforcement report+6 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 Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Methylcobalamin Injection Solution, 12.5mg/ml, packaged in 2 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Is Methylcobalamin Injection Solution, 5mg/ml recalled?

Yes. Northern VA Compounders P recalled Methylcobalamin Injection Solution, 5mg/ml on 30 Dec 2022. The recall is Class II and its status is Terminated. Recall number D-0119-2023.

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot#: 11292022@16, Exp 1/13/2023

Where was it sold?

Nationwide in the USA

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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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