Edge Pharma recalls 0.5mL eye drops due to potential contamination. This could cause infection if used. Check NDC 05446-0993-01 for affected products.
Lack of Assurance of Sterility
Edge Pharma is recalling a specific eye drop solution because it may not be sterile. Using this product could lead to eye infections if the solution is contaminated.
The eye drops may not be sterile, which means they could contain harmful bacteria. If the solution is contaminated, it might cause eye infections when used.
People who have the 0.5mL eye drop solution with NDC 05446-0993-01 are affected. Those with eye conditions or using the product for medical reasons are at higher risk.
Check for the NDC code 05446-0993-01 on the product label. The product was sold between December 2021 and February 2022.
Look for the NDC code 05446-0993-01 on the eye drop packaging.
The recall states there is a risk of contamination, so it is not safe to use. The product should be discarded.
Check for the NDC code 05446-0993-01 on the product label. The product was sold between December 2021 and February 2022.
The recall does not specify a remedy, so contact Edge Pharma directly for guidance.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0421-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0421-2022 from Edge Pharma. 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.
