Edge Pharma recalls sterile eye injection solution due to potential contamination risks. Affected units sold between Dec 2021 and Jan 2022. Consumers should contact the company for details.
Lack of Assurance of Sterility
Edge Pharma is recalling a specific eye injection solution because it may not be sterile. This could lead to infections if used improperly. The recall affects products sold in the US between December 2021 and January 2022.
The solution may not be sterile, which could cause infections if injected into the eye. This is a serious risk for medical procedures where the eye is involved.
People who have received this eye injection solution for medical use. Those with compromised immune systems are at higher risk of infection.
Check for the product name 'Moxifloxacin, Sterile Ophthalmic Solution for Injection, Preservative Free' with NDC 05446-1050-01. Products were sold between December 2021 and January 2022.
Reach out to Edge Pharma at 856 Hercules Dr., Colchester, VT 05446 for specific instructions on handling the recalled product.
The recall indicates a potential lack of sterility, so it is not safe to use. Consumers should contact Edge Pharma for details.
Contact Edge Pharma directly for instructions on how to handle the recalled product.
The product was recalled between December 2021 and January 2022.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0410-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0410-2022 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.