State Food and Drug Administration: A batch of medical devices from Roche Diagnostics and Medtronic is being recalled

On November 16, the State Food and Drug Administration issued an announcement to notify General Electric Medical Systems, Medtronic, and Roche Diagnostics of the voluntary recall of some of their violating products. These include a full-body X-ray computed tomography system, a single-use knife head, and a myoglobin detection kit.

GE Medical Systems, LLC Voluntarily Recalls Whole Body X-ray Computed Tomography Systems and Other Products

General Electric Medical Systems Trade Development (Shanghai) Co., Ltd. reported that due to the specific model and batch of products involved, if the SmartStep option is used during interventional procedures, the wrong dose may be displayed. The manufacturer General Electric Medical Systems Limited The company GE Medical systems, LLC voluntarily recalled products such as the whole body X-ray computed tomography system (registration number: National Machinery Injection 20143065741). The recall level is two.

Medtronic Xomed, Inc. Actively Recalls Disposable Blades and Other Products

Medtronic (Shanghai) Management Co., Ltd. reported an increase in fracture and wobble/vibration-related complaints due to specific models, specific batches of products, and manufacturer Medtronic Xomed, Inc. Products such as Blades for sexual use (registration number: National Machinery Injection 20162042506) are voluntarily recalled. The recall level is two.