Class II · Moderate risk Terminated
Cholecalciferol
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
CHOLECALCIFEROL Capsule
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Labeling: Label Mixup; CHOLECALCIFEROL Capsule, 50000 units may be potentially mislabeled as FENOFIBRATE, Tablet, 54 mg, NDC 00378710077, Pedigree: AD60272_64, EXP: 5/22/2014.
What was recalled
CHOLECALCIFEROL Capsule, 50000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 53191036201
- Recalling firm
- Aidapak Services, LLC
- Origin
- WA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-610-2014
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.
Other Cholecalciferol recalls
See all
Class II · Moderate risk Terminated
Vitamin D3 Cholecalciferol 50
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Class II · Moderate risk Terminated
Vitamin D3 Cholecalciferol 50
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Class II · Moderate risk Terminated
Cholecalciferol
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Cholecalciferol
Reason Lack of Assurance of Sterility
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