FDA alert: All sterile drug products of Med Prep Consulting recalled due to contamination

FDA alerts health care providers of recall of all sterile drug products by Med Prep Consulting in New Jersey

The U.S. Food and Drug Administration is alerting health care providers and patients of a voluntary nationwide recall of all lots of all products produced by Med Prep Consulting Inc. of Tinton Falls, N.J, a specialty pharmacy licensed by the state of New Jersey. The recall was announced after health care providers at a hospital in Connecticut observed floating particles, later identified to be a fungus, in five bags of magnesium sulfate intravenous solution.

The magnesium sulfate products may have been distributed to additional facilities in Connecticut, New Jersey, Pennsylvania, and Delaware. Until further notice, health care providers should stop using all products made by Med Prep Consulting Inc. and return them to the company.

"Giving a patient a contaminated injectable drug could result in a life-threatening infection," said Janet Woodcock, M.D., director of FDA's Center for Drug Evaluation and Research. "We do not have reports of patient infections. However, due to a lack of sterility assurance at the facility and out of an abundance of caution, this recall is necessary to protect patients."

This investigation is ongoing. The FDA is working with the Centers for Disease Control and Prevention and state officials in New Jersey and Connecticut to determine the scope of the contamination. The level of recall is to the user level, this includes regional hospital pharmacies and related departments, and physician's office practices. This recall includes all products distributed through March 15, 2013.

In addition to the recall, on March 15, 2013, the New Jersey State Board of Pharmacy entered into an Interim Voluntary Consent Order with Med Prep Consulting Inc. Under the Order, the firm has temporarily halted all production operations, including the processing and shipping of medications.

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