Recall Register

Food, drugs, devices › Firms

Nomax Inc

FDA recalling firm · 3 enforcement events · 8 product records · 2015–2024 · MO

Nomax Inc has 3 FDA enforcement events on this register (8 product records) between 2015 and 2024: 3 drug; the busiest year was 2015 with 1.

0% of its events are Class I; the most common class is Class III (2). 1 event is listed as ongoing; the recalling firm's address is in MO.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
19 Apr 2024GloStrips, Fluorescein Sodium Ophthalmic Strips USP (0.6 mg Fluorescein), Rx Only, a) 100 strips per carton, NDC 51801-003-40; b) 300 strips per carton, NDC 51801-003-50, Nomax, Inc., St. Louis, MO 63123.DrugClass II4Ongoing
13 Apr 2021Dry 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: 51801-008-15DrugClass III1Terminated
24 Mar 2015Fluorescein Sodium Ophthalmic Strips USP, 0.6 mg per strip, labeled as 1) Fluorescein GloStrips, individually wrapped strip (NDC 51801-003-01), barcode (01)00351801003012, packaged in a) 100-count strips per carton (NDC 51801-003-40, UPC 3 51801 00340 1); and b) 300-count strips per carton (NDC 51801-003-50, UPC 3…DrugClass III3Terminated

By type and class

Drug3
Class III2
Class II1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

15
16
17
18
19
20
21
22
23
24
25
26
Enforcement events for Nomax Inc by year initiated.

Questions and answers

How many FDA recalls has Nomax Inc had?

3 enforcement events (8 product records) on this register, 2015–2024: 3 drug.

Are any Nomax Inc recalls ongoing?

1 event is listed as ongoing in the current openFDA export.

What class are Nomax Inc recalls?

2 Class III, 1 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.