OFweek Medical Technology Network January 27 news, CFDA issued a recall announcement, Philips, Medtronic on the list. Philips (China) Investment Co., Ltd. said that its production of the control defibrillator [National Food and Drug Administration (Jin) word 2013 No. 3210458] was recalled due to abnormal work. This product is mainly used to terminate the patient's tachycardia and systolic symptoms, and can be used for AED treatment and manual asynchronous defibrillation therapy. It is understood that there are 3,751 products in China, of which 1,249 are inventories. Compared with the previous recall report, 31 new affected devices were added. The recall models are M3434A and M3556A. At the same time, Philips has also expanded the scope of the monitoring of defibrillators with M3535A and M3536A models. At present, there are 4 models of this model in China, one of which is inventories. Compared with the previous report, one additional affected equipment was added. In addition, since the anesthesia machine [National Food and Drug Administration (Jin) No. 2014 No. 3540770] may cause the patient to feel unwell, Philips recalled the product. At present, there are 51 products in China, of which 5 are in stock, and the production batch number is 21 batch numbers such as DK30100186, DK30100187 and DK30100188. Philips also said that there are still 35 affected ventilators in the Chinese market pending recall [Registration No.: SFDA(I) 20133540187], Medtronic and Confucius are within the scope of this recall. Medtronic (Shanghai) Management Co., Ltd. recalls nerve stimulation system and nerve stimulator [National Food and Drug Administration (into) word 2010 No. 3210663, National Food and Drug Administration (in) word 2010 No. 3261264, National Food and Drug Administration (in) word 2010 No. 3210392]. According to the company, the data may be inaccurate when the product uses certain parameter settings to enable cyclic stimulation. At present, there are 309 products in China, involving models 3023, 3058, and 7425. Kang Fusheng (Shanghai) Trading Co., Ltd. said that the company's four ventilators (registration number: SFDA (I) 20133543364) products are defective and recalled. Its serial numbers are BBV03936, BBV03939, BBV06598, BBV06611. Greenhouse Film Electric Roll Up The Greenhouse Film Manual Roll Up Unit can roll up a length of 60-80 meter, running stably with fine out side looking and long time of usage. The inside drive gears are made of high quality steel with fine workmanship, and what is more, there is lubricating bearing assembled on the out put and input shaft. At the meantime, there is also a group of reverse gear added to it. All these make the unit to be light and easy for Greenhouse Film Electric Roll Up,Roll Up Curtain Greenhouse,Greenhouse Film Vent Roller,Greenhouse Roll Up Motor JIANGSU SKYPLAN GREENHOUSE TECHNOLOGY CO.,LTD , https://www.alibabagreenhouse.com