I. General recall 1195 magnetic resonance imaging systems
General Electric Medical said that the casters of some specific Engstrom ventilators are more likely to be damaged. The damaged casters may cause the ventilator to fall or tilt (loss). The ventilator's fall/tilt may cause the patient or clinical staff. Serious injury. The company recalled a ventilator model named Engstrom Carestation, which currently has 86 units in China.
In addition, the company claims that in some locations, the MRU (magnet quench device) may not be connected to the magnet, which will cause the MRU to fail to perform its intended function and will not be able to quench the magnet when the user presses the button. The company will recall a magnet quench device of the type Singa Contour, which currently sells 1,195 units in China.
Second, Philips recalled X-ray computed tomography equipment, etc.
Philips Medical said that the company will recall 44 X-ray computed tomography equipment [Registration No.: National Food and Drug Administration (quasi) word 2013 No. 3301488, National Food and Drug Administration (quasi) word 2014 No. 3300672, national food and medicine The name of the mechanical (quasi) word 2013 No. 3300671] is due to the fact that the patient support device may accidentally move due to the failure of the vertical motor and the brake device. It is understood that the product is produced or imported in China with a total of 44 units.
At the same time, the medical angiography X-ray system of the model 722003 was incorrectly assembled due to the assembly of the suspension system of the display. The company recalled it and the product is currently sold in China.
In addition, the digital mammography machine of the model MultiDiagnost Eleva FD 702037 has product defects, affecting the normal use of the product, and the company recalls it. The product is currently sold in China.
3. Johnson & Johnson recalls tools and surgical instruments for craniofacial surgery
Johnson & Johnson said that the original batch number of MatrixMANDIBLE recoilers may have failed and/or corroded due to the use of springs made of incorrect raw materials; if the affected product does not work during the procedure and needs to be replaced, it may be Damage caused, the company recalled the external tool with the product model number 397.232.
In addition, the company's product model 329.143 cranial and maxillofacial surgical instruments are also flawed, the company recalled this.
Fourth, Stryker recalled small battery bone power mobile phone battery box, etc.
Stryker said that the company's small battery bone-powered mobile phone (registration number: National Food and Drug Administration (into) word 2014 No. 2102218) and bone power system (registration number: National Food and Drug Administration (in) word The battery case in 2014 No. 2102800 may be defective and the company recalls it. The model number is 6162-120-000, and the product is not currently sold in China.
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