On August 19th, the Beijing Food and Drug Administration issued two recall notices in China, involving the medical device products of Stryker and Holloj, respectively, with a recall level of three. In August, the recall of products in China's medical device market, together with the latest two announcements by the Beijing Food and Drug Administration, has reached a total of 28 cases involving Medtronic, Michael, Philips, Orson, Soling Diagnostics, Love 17 foreign-invested medical device companies including Kefa, Mérieux, PerkinElmer, Angola, Berenger, Bard, Roche, Wolfen, Xerox, Mani, Stryker and Holloch, and Shanghai Medical Devices Co., Ltd. Dental Materials Factory, a domestic medical device manufacturer. Among them, the 26 recalls previously issued details, micro-friends can click to read the old draft of Saibai blue equipment, "16 enterprises and 26 medical equipment recalls, all available in China (with list and details)." The following are the latest two recall details issued by the Beijing Bureau: 1. Howmedica Osteonics Corp. actively recalls joint surgery tools Stryker (Beijing) Medical Devices Co., Ltd. reported that the factory received four reports of separation of components related to the shin-clamp tool. The investigation found that the press-fit between the bone needle and the gripper sub-assembly did not meet the specifications, etc., the joint surgery tool produced by Howmedica Osteonics Corp. (registration or record number: National Food and Drug Administration (Jin) word 2013 1104042 No.) Proactive recall. The recall level is three.
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