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Medication Safety Alerts

Adrucil® 50 mg/mL Carton of 5 vials Voluntary Recall

09/04/2015

On September 4, 2015, the United States Food and Drug Administration (FDA) issued a notice regarding a voluntary recall of Adrucil® 50 mg/mL Carton of 5 vials. This recall was issued because it may contain silicone rubber particles. Using product 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 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 right-hand 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.

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.

If you are currently using Adrucil 50 mg/mL Carton of 5 vials and have questions regarding this recall, please call your doctor or call Teva Medical Information toll-free at 1‑888‑838‑2872. 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.accessdata.fda.gov.

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