Johnson & Johnson Vision Care, Inc. is recalling 114,165 ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses due to defects including bubbles or voids identified during product testing. These defects can interfere with the lens surface and potentially cause physical discomfort or eye injury during use. The recall affects specific daily-use lenses sold in 5-pack, 30-pack, and 90-pack configurations across various prescription strengths. Consumers should check their packaging for specific lot numbers to see if their supply is included in this voluntary recall.
The presence of bubbles or voids on the surface of the contact lens can cause eye irritation, pain, or potential injury to the cornea when the lens is worn. No injuries have been reported to date, but the defects were identified as a safety risk during standard finished goods testing.
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Quantity affects 114,165 lenses across these specific production lots.
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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