c20h10na2o5 fluorescein sodium ophthalmic stripsdrugHigh PriorityActive

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,

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, was recalled because lack of assurance of sterility: products have not been manufactured in conformance with current good manufacturing practices.. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified March 15, 2026.

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Key facts

Date announced: March 4, 2026
Source agency: FDA

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

What's Being Recalled

Quoted source excerpt from the official notice.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand: C20h10na2o5 fluorescein sodium ophthalmic strips
Category: drug
Source agency: FDA
Announced: March 4, 2026
Country: US
Status: Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

All lots

#	Model
1	All lots

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

1Stop using the affected product until you verify whether your item is impacted.
2Check the official recall notice and match your model, lot, or serial details.
3Follow the official instructions for repair, replacement, refund, or disposal.

Open Official Recall Notice

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: March 4, 2026
Last reviewed by RecallRadar: March 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists All lots.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the c20h10na2o5 fluorescein sodium ophthalmic strips recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/drug/enforcement.json?search=recall_number:D-0350-2026&limit=1

Keep browsing with these internal hubs: c20h10na2o5 fluorescein sodium ophthalmic strips recall hub and Food & Drug recall hub.