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Medication Safety Alerts

Baxter Injectable Products Voluntary Recall

07/16/2015

On July 16, 2015, the United States Food and Drug Administration (FDA) issued a notice regarding a voluntary recall of various injectable products manufactured by Baxter Healthcare. This recall was issued because of particles floating in the solution. Using solution containing particles may cause serious health problems.

This may represent a potential health hazard or safety risk to plan members who may be using product affected by this recall.

A complete list of the affected products and lot numbers is provided here:

To see if you have affected product, please check the lot number. The lot number can be found on the top left side of the manufacturer’s label. If your product is not from one of the affected lots, it is not affected by this recall. If your product is from one of these affected lots, please return it to the pharmacy that filled your prescription.

You should not continue to use product that is affected by this recall. Please call your doctor right away for advice if you may be using affected product. Your doctor is familiar with your medical history and can suggest the best treatment option for you. If you need a prescription for a different medicine, please call your doctor.

CVS/caremark Response: Please note: These products are not carried by the CVS/caremark Mail Service Pharmacies.

For more information, please call Baxter Healthcare toll-free at 1-888-229-0001, Monday through Friday, 7:00 am (CT) through 6:00 pm (CT). You may also call the FDA consumer inquiry line toll-free at 1‑888‑INFO-FDA (1‑888-463-6332) or visit their Web site at www.fda.gov.

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