Medline Industries, LP is recalling 3,116 medical convenience kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The recall was issued because the laryngoscope handles may fail to illuminate as intended. These kits were distributed to healthcare facilities in Alabama, California, Delaware, Oregon, Tennessee, and Texas.
If the laryngoscope light fails to turn on during a medical procedure such as intubation, it can cause a significant delay in patient care. Such delays in emergency airway management can lead to serious patient injury or death.
Contains Flexicare BritePro Solo Fiber Optic Laryngoscope Handles.
Contains Flexicare BritePro Solo Fiber Optic Laryngoscope Handles.
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.