Olympus Corporation of the Americas is recalling 984 units of Duravent Silicone Ventilation Tubes because the packaging may contain the incorrect device. Specifically, some packages for model 240075 may actually contain 1.32 mm Tiny T Tubes (model 70240076) instead. This recall involves lot numbers SM405666 and JB362646. No incidents or injuries have been reported to date.
If an incorrect ventilation tube is used during ear surgery, the patient may receive a device that is the wrong size or type. This can lead to surgical delays, the need for additional corrective medical procedures, or direct injury to the patient's ear canal.
Potential to contain model 70240076 (Tiny T Tubes) instead of the intended product.
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
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.