Linkbio Corp. has recalled 5 units of its CORE Workstation, a component used within the CORE Shoulder System. The workstation may display an incorrect "Planning Date" when medical staff are viewing patient cases on the "Start Case" menu screen. This voluntary recall affects devices distributed in Alabama, Florida, and Kansas, with no injuries or incidents reported to date.
The display of an incorrect planning date could lead to confusion or the use of outdated surgical plans, potentially impacting the timing or coordination of medical procedures.
All serial numbers of the CORE Workstation are affected.
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.