Product Compliance
Test/Filing/Registration
Johnson(Shanghai)Report of medical equipment Co., Ltd,Due to the products involved, there may be some adverse events such as washer not being cut and nailing,manufacturerEthicon Endo-Surgery, LLCCurved and straight intracavitary staplers Registration Certificate No National machinery injection20152652249 Endoscopic curved endovascular stapler Registration Certificate No National machinery injection20152650241 voluntary recall .Relevant product recall information has been published on2019year4month11Daily release,The recall level is level II.The recall level is now changed to level I,And change the sales quantity and corrective actions of the involved products in China.Name of product involved Code of registration certificate or filing certificate model For details such as specifications and batches, see Medical device recall event report form .
enclosure Medical device recall event report form
State Food and Drug Administration
2019year5month30day