Baxter Healthcare Corporation is recalling 2 units of the Welch Allyn Connex Spot Monitor because copper tape was improperly placed on the back of the device's liquid-crystal display. This manufacturing defect occurred during the assembly of the monitor's screen component. These specific monitors were distributed within the state of California. Consumers should contact the manufacturer or their healthcare provider to discuss how this defect may impact device performance and to coordinate a remedy.
The improper placement of copper tape on the back of the display screen may interfere with the device's electronics or display performance, potentially leading to incorrect readings or monitor failure.
Manufacturer or Healthcare Provider Consultation
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.