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Medication Safety Alerts

0.9% Sodium Chloride Injection 100 mL MINI-BAG VIAFLEX Container Voluntary Recall

09/04/2015

On September 4, 2015, Baxter Healthcare issued a notice regarding a voluntary recall 0.9% sodium chloride injection 100 mL MINI-BAG VIAFLEX container manufactured by Baxter Healthcare. This recall was issued because mold was found inside the overpouch. The overpouch is the pouch the IV bag is packaged in.

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

This recall affects lot number P329821 exp. 08/31/16. To see if you have affected product, please check the lot number. The lot number is located on the individual product or shipping carton. If your product is not from lot number P329821, it is not affected by this recall. If your product is from lot number P329821, please return it to the pharmacy that filled your prescription.

Please call your doctor right away for advice if you may be using affected product or if you do not know if you used affected product or not. 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: This product is not carried by the CVS/caremark Mail Service Pharmacies.

For more information, please call Baxter Healthcare Center for Service toll-free at 1‑888‑229-0001, Monday through Friday, 7:00 am to 6:00 pm (CT). You may also call the United States Food and Drug Administration (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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