Class II · Moderate risk Ongoing
Liceout
Reason CGMP violations.
Cyclosporine 1% Human Eye Drops
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Process Controls
What was recalled
Cyclosporine 1% Human Eye Drops, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-2776-92
- Recalling firm
- Westlab Pharmacy, Inc. dba Westlab Pharmacy
- NDC code
- 10002-2776-92
- Origin
- FL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0091-2019
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 Human recalls
See all
Class II · Moderate risk Ongoing
Liceout
Reason CGMP violations.
Class II · Moderate risk Completed
Sterile Diluent
Reason CGMP Deviations
Class II · Moderate risk Ongoing
Humanrace Suncare
Reason Subpotent Drug: Product does not contain SPF that is declared on the label.
Class II · Moderate risk Ongoing
Humanrace Suncare
Reason Subpotent Drug: Product does not contain SPF that is declared on the label.
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