Edge Pharma recalls sterile eye drops with potential contamination risk. Consumers should check NDC 05446-0815-01 for affected products.
Lack of Assurance of Sterility
Edge Pharma is recalling a specific eye drop solution due to a lack of assurance of sterility. This means the product could be contaminated, posing a risk of infection if used.
The product lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. Using contaminated eye drops might lead to eye infections or other complications.
People who purchased the specific eye drop solution from the listed manufacturer. Those with sensitive eyes or using the product for medical reasons may be at higher risk.
Check for the NDC code 05446-0815-01 on the product label. The product was sold starting December 28, 2021, and is a multiple-dose droptainer for eye use.
Look for the NDC code 05446-0815-01 on the dropper bottle.
The recall states there is a lack of assurance of sterility, so the product may be contaminated. Do not use until you confirm it's not recalled.
Check the product label for the NDC code 05446-0815-01. If it matches, stop using it and contact Edge Pharma for guidance.
The recall record does not mention a replacement or remedy, so contact Edge Pharma directly for assistance.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0420-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0420-2022 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.