More than 20 equipment companies take the initiative to recall the product

Pharmaceutical Network January 16 hearing recently, the State Food and Drug Administration released a message, more than 20 companies take the initiative to recall medical device products.
Akei Lai International Trade (Shanghai) Co., Ltd. reported that due to its proxy Of the glucose test strips (enzymatic) enzyme content is low, affecting the test results, test paper manufacturer ARKRAY Factory, Inc. on its production of glucose test strips (enzymatic) 'State Food and Drug Administration (into) 2014 No. 2400688 'Take the initiative to recall the recall level of one.
Toshiba Medical Systems (China) Co., Ltd. on the medical angiography X-ray machine 'State Food and Drug Administration (into) 2014 No. 3302979, the State Food and Drug Administration (into) 2014 No. 3302978, State Food and Drug Administration Into the word 2011 No. 3303868 'initiative to recall. Johnson & Johnson (Shanghai) Medical Equipment Co., Ltd. on the hip joint surgery tools (State Equipment No. 20160321) initiative to recall Roche Diagnostics (Shanghai) Co., Ltd. on the modular biochemical immunoassay system Guo-li injection into the 20173406307), automatic biochemical immunoassay analyzer (Guo-li injection into 20153401247), automatic chemiluminescence immunoassay analyzer 'State Food and Drug Administration (into) word 2014 No. 3404503, the State Food and Drug Administration ( Into) the word 2006 No. 3400500 'initiative to recall.Kook (China) Medical Trading Co., Ltd. tubal catheterization device (state injection into 20143665597) take the initiative to recall the recall target only Guangzhou Mokai medical instruments Co., Ltd. and customers who purchased the recalled batches from Guangzhou Meikai Medical Devices Co., Ltd. Kang Er Fusheng (Shanghai) Trading Co., Into) 2003 No. 2540384 'initiative to recall. Hengjia Medical Devices Trading (Shanghai) Co., Ltd. on the spiral CT radiation therapy system' State Food and Drug Administration (into) 2012 No. 3322426 (more) ', spiral CT and radial irradiation Treatment system 'State Food and Drug Administration (into) word 2012 No. 3332427' take the initiative to recall the above product recall levels are two.
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