The FDA announced that Teleflex, and their subsidiary Arrow International, are recalling the ARROW Endurance Extended Dwell Peripheral Catheter System after reports of catheter separation or leakage. Teleflex/Arrow International reports 83 complaints related to this issue. There have been 18 reported injuries and no deaths, the FDA stated, noting that the agency has identified this as a Class I recall, the most serious type of recall. “Use of these devices may cause serious injuries or death,” stated the FDA in its recall notice, which indicates the date the recall was initiated by the firm as May 19, 2023.
Published first on TheFly
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