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Medication Safety Alerts

Mibelas™ 24 Fe tablets Voluntary Recall


On May 26, 2017, Lupin Pharmaceuticals, Inc. issued a voluntary recall of MibelasTM 24 Fe tablets. This recall was issued due to a packaging error. As a result of this packaging error, women could be at risk for unintended pregnancy.

An example of the tablets is the proper order is provided here:

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 L600518 exp. 05/31/18. To see if you have affected product, please check the lot number. The lot number is located on the right hand side of the manufacturer’s carton or on the back side of the wallet. If your product is not from lot number L600518, it is not affected by this recall. If your product is from lot number L600518, 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. 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: If you are currently taking Mibelas 24 Fe tablets, please call a Customer Care representative toll-free at 1-866-823-5184. We will give you more information and help with arrangements for the return and replacement of any affected product.

If you are currently taking Mibelas 24 Fe tablets and have questions regarding this recall, please call your doctor or call Lupin Pharmaceuticals, Inc toll-free at 1‑866‑587‑4617.You may also call the U.S. Food and Drug Administration (FDA) consumer inquiry line toll-free at 1‑888‑INFO‑FDA (1‑888‑463‑6332) or visit

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