US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 4, 2017 (9 years ago)

Doxercalciferol Capsules 0.5mcg

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print.

What was recalled

Doxercalciferol Capsules 0.5mcg, 50 count bottles, Rx, only, Manufactured by Cipla Limited Kurkumbh, Maharashtra, India, Manufactured for West-Ward, Pharmaceuticals, Corp., Eatontown, NJ -- NDC 0054-0338-19

Recalling firm
West-Ward Columbus, Inc.
NDC code
0054-0338-19
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0651-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.