CLASS II Drug recall · Reported 22 May 2013 · FDA Enforcement Report

Methylcobalamin (Buffered) Injection,1 mg/mL vial recalled

NuVision Pharmacy is recalling Methylcobalamin (Buffered) Injection,1 mg/mL vial, Stock# 11126, Preservative Free, distributed in Florida, Missouri, Utah, Washington. The recall was initiated on 28 Mar 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number N01232013@4, Do Not Use Beyond Date of January 1, 2014
Quantity recalled32 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-417-2013
FDA event ID
64722
Recalling firm
NuVision Pharmacy, Dallas, TX
Classification
Class II
Status
Terminated
Recall initiated
28 Mar 2013
FDA classified
16 May 2013
Reported
22 May 2013
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

28 Mar 2013Recall initiated by company
16 May 2013Classified by FDA+49 days
22 May 2013Published 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; reports of adverse events after injection

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 (Buffered) Injection,1 mg/mL, 30 mL vial, Stock# 11126, Preservative Free, Compounded by NuVision Pharmacy, Inc., Dallas, TX 75244

Where it was distributed

FL, MO, UT, and WA.

FloridaMissouriUtahWashington

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility; reports of adverse events after injection

Which lots are affected?

Lot Number N01232013@4, Do Not Use Beyond Date of January 1, 2014

Where was it sold?

FL, MO, UT, and WA.

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.

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