Approximately 5,476 bottles of Betimol (timolol ophthalmic solution) 0.5% have been recalled because the product may lack assurance of sterility. The 15mL bottles were found to be out of specification for volume and may have compromised container seals. No injuries or incidents have been reported in connection with this recall.
A compromised container seal can allow bacteria or other contaminants to enter the bottle, potentially causing serious eye infections. This is especially concerning for ophthalmic products used directly in the eye.
You have 2 options:
Rx only product manufactured for Thea Pharma Inc.
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 ยท Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.