Maquet GmbH has recalled 315 Corin Operating Tables (8 in the U.S.) because the device may become unresponsive during use. The recall was initiated because simultaneous use of the table with other medical tools, specifically high-frequency (HF) surgical equipment, can cause electronic interference. If this interference occurs, the table will not respond to commands from the universal remote control or the manual override panel.
If the operating table becomes unresponsive while a patient is being positioned or during an active surgical procedure, it could result in surgical delays or unintentional patient movement, potentially leading to patient injury.
Recall affects all units associated with listed Serial Numbers and UDI-DIs across the six designated model numbers.
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.