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Medication Safety Alerts

Eyesaline Eyewash Voluntary Recall

12/28/2016

On December 28, 2016, the United States Food and Drug Administration (FDA) issued a notice regarding a voluntary recall of Eyesaline Eyewash manufactured by Honeywell. This recall was issued because the product could have bacteria that may cause an infection that could affect your vision.

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 F16091-61 exp. 03/19. To see if you have affected product, please check the lot number. The lot number can be found on the outside of the product case and on individual bottles. If your product is not from lot number F16091-61, it is not affected by this recall. If your product is from lot number F16091-61, please contact the pharmacy that filled your prescription for further instructions.

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 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 Eyesaline Eyewash and have questions regarding this recall, please call your doctor or call please call Honeywell Customer Care toll-free at 1‑800‑430-5490, Monday through Friday, 8:00 am through 6:30 pm (ET).  You may also call the FDA consumer inquiry line toll-free at 1‑888‑INFO-FDA (1‑888-463-6332) or visit https://www.accessdata.fda.gov.

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