Nomax recalls GloStrips eye drops due to impurities in the fluorescein sodium. These strips may cause eye injury if used. Affected lots expire by June 2024. Contact for return instructions.
Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP monograph in regard to Unspecified Impurities.
Nomax is recalling GloStrips eye drops because they contain impurities that could harm your eyes. This recall affects specific lots that expire by June 2024. The product is prescription-only and must be returned if you have it.
The eye drops contain impurities that could cause eye injury when used. This happens because the product doesn't meet the required purity standards for safe medical use.
Prescription eye drop users who have the recalled GloStrips lots (expiring June 2024) are most at risk. Patients using these strips for eye tests may experience eye injury.
Check the carton for 'GloStrips, Fluorescein Sodium Ophthalmic Strips USP (0.6 mg Fluorescein), Rx Only'. Look for specific lot numbers: 14904 (expiring June 30, 2024), 14938 (expiring July 31, 2024), or 14931 (expiring June 30, 2024).
Look for lot numbers 14904, 14938, or 14931 on the carton label.
Contact Nomax Inc for instructions to return the product if you have the recalled lots.
No, the recalled lots contain impurities that could cause eye injury. Do not use these products.
Check the carton for lot numbers 14904 (expiring June 30, 2024), 14938 (expiring July 31, 2024), or 14931 (expiring June 30, 2024).
Contact Nomax Inc for instructions to return the product. Do not use the recalled lots.
We’ve drafted a message you can send Nomax to request your refund or repair — edit it as you like.
Subject: Recall D-0462-2024 — Nomax Nomax Hello, I own a Nomax that is covered by recall D-0462-2024 from Nomax. 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.
