US Drug Recall Register
Class III · Low risk Terminated Initiated Jul 11, 2019 (7 years ago)

Gatifloxacin Ophthalmic Solution 0.5%, For Use in the Eyes Only, Rx Only, Sterile, 2.5 mL…

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

Why it was recalled

Labeling: Missing label; Product complaints reported missing bottle label.

What was recalled

Gatifloxacin Ophthalmic Solution 0.5%, For Use in the Eyes Only, Rx Only, Sterile, 2.5 mL Bottle, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India, NDC 68180-435-01.

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-435-01
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1490-2019

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.

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