Dec 20 (Reuters) - FDA:
2023年12月20日(路透社) - FDA:
FDA: ICU Medical Removes Some Csb Batteries Intended for Use With Plum 360, a+, and a+3 Infusion Systems - Website
FDA: ICU Medical Recall Involves Removing Some Devices From Where They Are Used/Sold; Identified Recall as Most Serious Type
FDA: ICU Medical Recalls Some Csb Batteries Intended for Infusion Pumps Over Reports of Alleged Counterfeit Counterfeit, Untested Batteries in Use
FDA:ICU醫療移除了一些用於Plum 360、a+和a+3輸注系統的Csb電池 - 網站
FDA:ICU醫療召回涉及從使用/銷售地點移除某些設備;已將召回識別爲最嚴重類型
FDA:ICU醫療召回部分用於輸液泵的Csb電池,因報告使用了涉嫌假冒、未經測試的電池。
Further Company Coverage: Icui.o
進一步公司報道: Icui.o
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