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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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FDA clarifies policies for compounders as national GLP-1 supply begins to stabilize
[2/21/2025] FDA has determined the shortage of semaglutide injection products, a glucagon-like peptide 1 (GLP-1) medication, ...
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Do not purchase or use Skin-Cap Aerosol Spray Products because they may be harmful to your health.
[10/30/2024] FDA is warning consumers to not purchase or use Skin-Cap aerosol spray products because they may contain undisclosed steroids. this ...
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FDA warns patients and health care professionals not to use compounded drugs from Fullerton Wellness
[11/1/2024] FDA is warning patients and health care professionals not to use drugs compounded and distributed by Fullerton Wellness LLC, Ontario, ... ...
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FDA warns health care professionals not to use epinephrine nasal solutions from BPI Labs and Endo USA
[1/16/2025] FDA is warning health care professionals not to use unapproved epinephrine nasal solutions manufactured by BPI Labs LL...
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FDA warns consumers not to use SnoreStop Nasal Spray by Green Pharmaceuticals due to potential contamination
[9/18/2024] FDA is warning consumers and health care professionals not to use SnoreStop Nasal Spray, distributed by Green Pharmaceuticals Inc. ...
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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…
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