February 2018 33 Medical Device Recalls | Multiple large enterprises involved
According to the CFDA open data, a total of 33 medical devices were recalled in February 2018, down significantly from 108 in January, which may be affected by the Spring Festival holiday.
Secondary recalls are foreign companies
In February's recall, the second-level recall was 9 and all the manufacturers involved were foreign investors enterprise , Including Philips, GM, Roche, BDI and Celestial.
There are two Roche second-level recalls, the recall of products with diagnostic reagents and urine analyzer, Roche had three recalls in January.
Table 1: Secondary Recalls in February
Involved in multiple large enterprises
In the third-level recall, it also involves many domestic and foreign large enterprises such as Mindray's Blood Analyzer, Siemens Diagnostic and Nuclear Magnetic Resonance Systems, Abbott's kit, and Baxter's treatment kits.
There are a variety of reasons for recalls, package stickiness issues, incorrect labels, product content, software problems, and nonconformities standard Requirements and so on.
Recall products, the diagnostic equipment has 6, 6 diagnostic reagents, there are other breathing machine, bone and joint systems, catheters and so on.
