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Class I: serious health riskTerminated

Green Valley Drugs Cyanocobalamin 1000 mcg/ml Recall

Cyanocobalamin 1000 mcg/ml, injection 30 mL, MDV, For Office Use Only, Green Valley Dru…

Green Valley Drugs · Henderson, NV

Risk level
Class I
Reported by FDA
May 22, 2013
Recall ID
D-322-2013
Check your lot numberHow we source this data

Summary

Green Valley Drugs recalled Cyanocobalamin 1000 mcg/ml starting Dec 4, 2012. The FDA classified it as Class I (serious health risk) and published enforcement report D-322-2013 on May 22, 2013. Reason: Non-Sterility: Green Valley Drugs received positive sterility results from their testing lab on two lots of Methylprednisolone Preservative Free 40 mg/mL injectable suspension and one lot of Cyanocobalamin 1000 mcg/mL injection, 30 mL MDV. Status: Terminated.

Why it was recalled

Non-Sterility: Green Valley Drugs received positive sterility results from their testing lab on two lots of Methylprednisolone Preservative Free 40 mg/mL injectable suspension and one lot of Cyanocobalamin 1000 mcg/mL injection, 30 mL MDV.

Product description

Cyanocobalamin 1000 mcg/ml, injection 30 mL, MDV, For Office Use Only, Green Valley Drugs, Manufactured by Green Valley Drugs, Henderson, NV.

Lot numbers, UPCs & expiration codes

Lot: 20121126-H

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-322-2013
Classification
Class I
Status
Terminated
Recall initiated
Dec 4, 2012
FDA report date
May 22, 2013
Quantity
58 x 30 ml Vials
Recall type
Voluntary: Firm initiated
Recalling firm
Green Valley Drugs

Original FDA data

Every field from FDA enforcement report D-322-2013, exactly as published.

Show all FDA fields
City
Henderson
State
NV
Status
Terminated
Country
United States
Event ID
63953
Address
1850 Whitney Mesa Dr
Address (line 2)
Suite 180
Code information
Lot: 20121126-H
Postal code
89014-2091
Report date
May 22, 2013
Product type
Drugs
Recall number
D-322-2013
Classification
Class I
Recalling firm
Green Valley Drugs
Product quantity
58 x 30 ml Vials
Termination date
May 17, 2013
Reason for recall
Non-Sterility: Green Valley Drugs received positive sterility results from their testing lab on two lots of Methylprednisolone Preservative Free 40 mg/mL injectable suspension and one lot of Cyanocobalamin 1000 mcg/mL injection, 30 mL MDV.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cyanocobalamin 1000 mcg/ml, injection 30 mL, MDV, For Office Use Only, Green Valley Drugs, Manufactured by Green Valley Drugs, Henderson, NV.
Distribution pattern
Nationwide
Recall initiation date
Dec 4, 2012
Initial firm notification
Letter
Center classification date
May 15, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-322-2013, published May 22, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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