PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: May 26, 2021 Initiated: April 13, 2021 #D-0387-2021

Product Description

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

Reason for Recall

Subpotent Drug

Details

Recalling Firm
Nomax Inc
Units Affected
78 cartons
Distribution
Nationwide USA
Location
Saint Louis, MO

Frequently Asked Questions

What product 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. Recalled by Nomax Inc. Units affected: 78 cartons.
Why was this product recalled?
Subpotent Drug
Which agency issued this recall?
This recall was issued by the FDA Drug on May 26, 2021. Severity: Low. Recall number: D-0387-2021.