Wizcure Pharmaa recalls CHNaO Fluorescein Sodium Ophthalmic Strips (1mg) due to lack of sterility assurance in manufacturing. Products sold in 100-count and 300-count boxes with specific NDC numbers are affected.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Wizcure Pharmaa is recalling CHNaO Fluorescein Sodium Ophthalmic Strips because they were not made with proper sterility standards. This could lead to infections if used improperly. Affected products include 100-count and 300-count boxes with specific NDC numbers.
The product was not manufactured according to current good practices, which means it might not be sterile. Using non-sterile eye drops could cause infections or other eye issues, especially for people with sensitive eyes or medical conditions.
People who own or use the recalled CHNaO Fluorescein Sodium Ophthalmic Strips, particularly those with eye conditions requiring frequent use. Individuals using the product for medical purposes are at higher risk.
Check for the product name 'CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg' in 100-count or 300-count boxes. Look for NDC numbers 83851-100-10 or 83851-100-30 on the packaging.
Look for the NDC numbers 83851-100-10 or 83851-100-30 on the packaging to confirm if the product is recalled.
The product was not manufactured in conformance with current good manufacturing practices, which could lead to lack of sterility.
The official recall notice does not specify a remedy, so check the product details to see if it matches the recalled items.
The recall indicates a potential risk of infection due to lack of sterility, but the exact risk level is not specified in the notice.
We’ve drafted a message you can send Wizcure Pharmaa to request your refund or repair — edit it as you like.
Subject: Recall D-0350-2026 — Wizcure Pharmaa Wizcure Pharmaa Hello, I own a Wizcure Pharmaa that is covered by recall D-0350-2026 from Wizcure Pharmaa. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
