Johnson & Johnson (Shanghai) Medical will actively recall hollow screws and patches

According to the website of the State Food and Drug Administration, Johnson & Johnson (Shanghai) Medical Equipment Co., Ltd. recently voluntarily recalled the hollow screws and patches. The specific report is as follows:

I. Johnson & Johnson (Shanghai) Medical Equipment Co., Ltd. Report: The company has not registered hollow screws with pure titanium materials, and the hollow screws for the sale of pure titanium materials do not comply with Chinese regulations. The company voluntarily recalled related products. The recall level is Level III. Detailed information on the model, specifications and batches of the products can be found in the Medical Device Recall Report Form.

Second, Johnson & Johnson (Shanghai) Medical Equipment Co., Ltd. report: The company's research found that the recurrence rate or reoperation rate of the products involved was higher than the average recurrence rate of other patches. The company voluntarily recalled related products. The recall level is Level II. Detailed information on the model, specifications and batches of the products can be found in the Medical Device Recall Report Form.

Johnson & Johnson (Shanghai) Medical will actively recall hollow screws and patches

Johnson & Johnson (Shanghai) Medical will actively recall hollow screws and patches

Chemical Materials

Chemical Materials,Sodium Benzoate,Sodium Diacetate,Potassium Sorbate

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