Dry Eye Test — Class III drug recall D-0387-2021
Terminated recall by Nomax Inc, reported 2021-05-26, distributed nationwide. Subpotent Drug
| Recall number | D-0387-2021 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nomax Inc, Saint Louis, MO, United States |
| Recall initiated | 2021-04-13 |
| Classified | 2021-05-18 |
| Reported by FDA | 2021-05-26 |
| Terminated | 2023-09-28 |
| Distributed | Nationwide (US) |
| Quantity | 78 cartons |
| Reason classes | potency |
| NDC | 51801-0008, 51801-0008-15 |
| Lot numbers | 07/23, 13336 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0387-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.