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Medtronic, Inc. initiates recall of single-use intracardiac diagnostic electrode catheters (2025-02-25)
Index No. JGXX-2025-118 Subject Classification Regulatory Information / Ordered Recall Information Title Beckman Coulter (U.S.A.) Inc Beckman Coulter, Inc. is voluntarily recalling its fully automated chemiluminescent immunoassay analyzer Issue Date 2025-02-25 Beckman Coulter Trading (China) Co. Ltd. is reporting that due to the product's Z-axis pallet clamping motor A forced stop resulted in a c...
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Medtronic, Inc. initiates recall of single-use intracardiac diagnostic electrode catheters (2025-02-25)
Index No. JGXX-2025-114 Subject Classification Regulatory Information / Ordered Recall Information Title Medtronic, Inc. initiated a voluntary recall of single-use intracardiac diagnostic electrode catheters Release Date 2025-02-25 Medtronic (Shanghai) Management Co. Ltd. has reported that due to the presence of an incorrect model number and batch number on the product's outer box labeling, the manufacturer, Medtronic, Inc. Medtronic, I...
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Oridion Medical 1987 Ltd. voluntarily recalls micro-bypass end-expiratory carbon dioxide monitoring sampling tubes (2025-02-25)
Index No. JGXX-2025-117 Subject Classification Regulatory Information / Ordered Recall Information Title Oridion Medical 1987 Ltd. is voluntarily recalling micro-bypass end-expiratory carbon dioxide monitoring sampling tubes Release Date 2025-02-25 Kewe Medical Devices International Trading (Shanghai) Co. Ltd. is reporting that, due to the sampling tubes being removed from the patient's tracheal intubation...
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百多力股份有限公司BIOTRONIK AG对自膨式镍钛合金外周血管支架系统主动召回 (2025-02-25)
索引号 JGXX-2025-116 主题分类 监管信息 / 责令召回信息 标题 百多力股份有限公司BIOTRONIK AG对自膨式镍钛合金外周血管支架系统主动召回 发布日期 2025-02-25 百多力(北京)医疗器械有限公司报告,由于产品实物尺寸与包装标识不一致的原因,生产商百多力股份有限公司BI…