Nutrifill Physiologic formula Contact Lens Insertion solution, manufactured by Contamac Solutions, Inc., is being recalled because the product may lack sterility. The recall affects 17,273 cartons containing 604,555 individual ampoules. Using non-sterile solution in the eyes can lead to serious health complications, although no incidents or injuries have been reported to date.
A lack of sterility in a solution applied directly to the eye can introduce harmful microorganisms. This poses a significant risk of eye infections, inflammation, or irritation, which in severe cases could impact vision.
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Quantity affected: 17,273 cartons (604,555 ampoules)
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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