CLASS II ONGOING Drug recall · Reported 4 Mar 2026 · FDA Enforcement Report
CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) recalled
Wizcure Pharmaa Private is recalling CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a), distributed nationwide in the US. The recall was initiated on 31 Dec 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0350-2026
- FDA event ID
- 98253
- Recalling firm
- Wizcure Pharmaa Private, Bhiwadi, N/A
- Manufacturer
- Vistamerica USA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 Dec 2025
- FDA classified
- 25 Feb 2026
- Reported
- 4 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Eye Drops
Timeline
| 31 Dec 2025 | Recall initiated by company | |
| 25 Feb 2026 | Classified by FDA | +56 days |
| 4 Mar 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) 100-count box, NDC 83851-100-10; b) 300-count box, NDC 83851-100-30. Manufactured by Wizcure Pharmaa PVT. LTD, H-681, Phase 3, RIICO Industrial Area, Bhiwadi- 301019 INDIA, Vistamerica USA, 20 Perkins Dr. Prescott, AZ 86301, Vistamerica USA, Made in India,
Where it was distributed
Distributed Nationwide in the USA
Questions about this recall
Why was it recalled?
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Which lots are affected?
All lots
Where was it sold?
Distributed Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
6 other products · FDA event 98253This product is part of a recall event; the main page for the event is BioGlo Fluorescein Sodium Ophthalmic Strips recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | BioGlo Fluorescein Sodium Ophthalmic Strips recalled | Wizcure Pharmaa Private | Sterility | Nationwide | |
| CLASS II | Bio Glo Fluorescein Sodium Ophthalmic Strips recalled | Wizcure Pharmaa Private | Sterility | Nationwide | |
| CLASS II | Vista Tears Polyethylene Glycol 400 0.4% w/v recalled | Wizcure Pharmaa Private | Sterility | Nationwide | |
| CLASS II | Vista Gel Hypromellose USP 0.3% w/v recalled by Wizcure Pharmaa PrivateVista Hypromellose Dry Eye Relief | Wizcure Pharmaa Private | Sterility | Nationwide | |
| CLASS II | Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant | Wizcure Pharmaa Private | Sterility | Nationwide | |
| CLASS II | Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recalledVista Meibo Tears Propylene Glycol 0.6% W/v Advanced Dry Eye Relief Lubricating Drops 10 Ml | Wizcure Pharmaa Private | Sterility | Nationwide |
More recalls from Wizcure Pharmaa Private
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recalledVista Meibo Tears Propylene Glycol 0.6% W/v Advanced Dry Eye Relief Lubricating Drops 10 Ml | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Vista Gel Hypromellose USP 0.3% w/v recalled by Wizcure Pharmaa PrivateVista Hypromellose Dry Eye Relief | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Vista Tears Polyethylene Glycol 400 0.4% w/v recalled | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Bio Glo Fluorescein Sodium Ophthalmic Strips recalled | Wizcure Pharmaa Private | Sterility | Nationwide |
Other Fluorescein recalls
All 8| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | GloStrips, Fluorescein Sodium Ophthalmic Strips recalled by NomaxGlostrips | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS II | GloStrips, Fluorescein Sodium Ophthalmic Strips recalled by NomaxGlostrips | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS III | Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips recalled by NomaxDry Eye Test | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS II | Altaire Fluorescein Sodium with Proparacaine Hydrochloride recalledFluorescein Sodium And Proparacaine Hydrochloride | Altaire Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Fluorescein/Indocyanine, Lyophilized (P.F.), 400 mg/15 mg recalled | Wells Pharmacy Network | Sterility | Nationwide |