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National Medical Products Administration: A batch of medical devices from Roche Diagnostics and Medtronic is being recalled.
Release time:
2022-01-18 17:24
On November 16, the National Medical Products Administration announced the active recall of certain non-compliant products by General Electric Medical Systems, Medtronic, and Roche Diagnostics. This includes whole-body X-ray computed tomography systems, single-use blades, and myoglobin test kits.
General Electric Medical Systems, LLC actively recalls whole-body X-ray computed tomography systems and other products.
General Electric Medical Systems Trading Development (Shanghai) Co., Ltd. reported that due to specific models and batches of products, there is a potential issue of incorrect dosage display when using the SmartStep option during interventional surgery. The manufacturer, General Electric Medical Systems, LLC, actively recalls whole-body X-ray computed tomography systems (registration number: 国械注进20143065741) and other products. The recall level is classified as Level 2.
Medtronic Xomed, Inc. actively recalls single-use blades and other products.
Medtronic (Shanghai) Management Co., Ltd. reported that due to specific models and batches of products, there has been an increase in complaints related to breakage and swinging/vibration. The manufacturer, Medtronic Xomed, Inc., actively recalls single-use blades (registration number: 国械注进20162042506) and other products. The recall level is classified as Level 2.
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