D-0387-2021 Class III Terminated

Recalled by Nomax Inc — Saint Louis, MO

FDA drug recall D-0387-2021 was initiated by Nomax Inc on April 13, 2021 and is designated Class III. Reason for recall: Subpotent Drug The recall status is terminated (terminated September 28, 2023). Affected quantity: 78 cartons.

Recall Details

Product Type
Drugs
Report Date
May 26, 2021
Initiation Date
April 13, 2021
Termination Date
September 28, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
78 cartons

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

Distribution Pattern

Nationwide USA

Code Information

LOT 13336 EXP 07/23