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Medication Safety Alerts

Intralipid 20 % Voluntary Recall

November 1, 2017

On November 1, 2017, the United States Food and Drug Administration (FDA) issued a notice regarding a voluntary recall of Intralipid® 20 % manufactured by Baxter Healthcare. This recall was issued because the product was exposed to temperatures below freezing while in transit.

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 10LE9597 exp. 04/01/19. To see if you received product from this affected lot, please check the lot number. The lot number is located on the front of the product under the bar code. If your product is not from lot number 10LE9597, it is not affected by this recall. If your product is from lot number 10LE9597,please contact the pharmacy that filled your prescription for more information.

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: this product is not carried by the CVS Caremark Mail Service Pharmacies.

If you are currently using Intralipid 20 % and have questions regarding this recall, please call your doctor or call Baxter Healthcare toll-free at 1-800-437-5176, Monday through Friday, 7:00 am to 6:00 pm (CT) or visit https://www.baxter.com/.

You may also call the FDA toll-free at 1‑888‑INFO-FDA (1‑888-463-6332) or visit https://www.accessdata.fda.gov/.

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