Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Subpotent Drug
Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15
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.
Reason Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Reason Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Reason Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Reason Subpotent Drug
Reason Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current…
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