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# Arrow Recalls Peripheral Catheter System
- URL: https://www.fdaweb.com/arrow-recalls-peripheral-catheter-system/
- Published: 2023-06-22T12:00:00.000Z
- Updated: 2026-09-14T18:40:29.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154743

Arrow International has recalled (Class 1) its Arrow Endurance Extended Dwell Peripheral Catheter System due to the potential for catheter separation or leakage. Last month, Arrow/Teleflex sent customers an “urgent medical device recall” letter instructing them to immediately discontinue using and quarantine the products, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=200606&ref=fdaweb.com). The notice says that there is no FDA-determined cause of the recall because it is still under investigation by the firm.