Nomax recalls GloStrips ophthalmic strips due to unspecified impurities in the active ingredient. This may affect safety for eye treatments. Check your product details to see if you need to take action.
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 ophthalmic eye drops because the active ingredient may contain impurities that don't meet safety standards. This could pose a risk to eye health if used improperly.
The active ingredient in the product may contain impurities that don't meet the required safety standards. This could lead to potential eye irritation or other adverse effects if the strips are used as intended.
People who have prescription ophthalmic strips from Nomax Inc. with the specific lot number 14708 are affected. Those using the product for eye treatments are most at risk.
Check for the product name 'GloStrips, Fluorescein Sodium Ophthalmic Strips USP (1.0 mg Fluorescein), Rx Only, 100 Sterile Strips per carton' on the packaging. Look for the lot number 14708 and expiration date 04/30/2024.
Identify the product name, lot number, and expiration date to confirm if it's recalled.
The recall record states that the active ingredient may contain impurities that don't meet safety standards, so it's not recommended to use the product.
The recall record does not specify a remedy, so you should check with Nomax Inc. for further instructions.
Look for the product name 'GloStrips, Fluorescein Sodium Ophthalmic Strips USP (1.0 mg Fluorescein), Rx Only, 100 Sterile Strips per carton' and the lot number 14708 with expiration date 04/30/2024.
We’ve drafted a message you can send Nomax to request your refund or repair — edit it as you like.
Subject: Recall D-0463-2024 — Nomax Nomax Hello, I own a Nomax that is covered by recall D-0463-2024 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.
