Nomax Inc recalls Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of…

Recall date

April 13, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0387-2021

FDA classification

Class III

Brand / firm

Nomax Inc

Sold / distributed

Nationwide USA

Why it was recalled

Subpotent Drug

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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