According to Article 78 of the Regulations for the Supervision and Administration of Medical Devices, if a medical institution violates the regulations and fails to implement measures such as recalling, stopping the use of, removing from the shelves, or reporting of medical devices, or fails to implement measures such as replacing or updating medical devices, the supervisory authority shall order rectification, and may impose fines and revoke the relevant license documents. The exact amount of the fine varies depending on the violation and can be affected by a number of factors, including the degree of violation, the scope of the impact, the degree of harm, and so on.
It is important to note that medical institutions need to strictly comply with relevant regulations and standards when using medical devices to ensure that they are safe and effective.