FDA IDENTIFIES CLASS I RECALL BY TELEFLEX ARROW ENDURANCE EXTENDED DWELL PERIPHERAL CATHETER SYSTEM
07/06/2023
On June 26, 2023, the U.S. Food and Drug Administration (FDA) identified a product recall by Teleflex and its subsidiary Arrow International for their product the ARROW Endurance Extended Dwell Peripheral Catheter System. The recall was first initiated by the firm on May 19, 2023, because of the risk of catheter separation and leakage. The FDA has identified this case as a Class I recall, the most...
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