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# ReFlow Recalls Wingman35 Catheters
- URL: https://www.fdaweb.com/reflow-recalls-wingman35-catheters/
- Published: 2017-05-03T12:00:00.000Z
- Updated: 2026-09-14T22:21:28.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5138607

FDA says that ReFlow Medical is recalling specified lots of its Wingman35 crossing catheters. An agency [notice](https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm556541.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery) says the catheters have been found to exhibit tip splitting or separation, which has resulted in two adverse events. Tip splitting has the potential to lead to loss of device function, the notice says, while tip separation may require medical intervention to retrieve a separated segment or may occlude blood flow to end organs.

The catheters being recalled were distributed between 1/2015 and 3/2016\. The company reportedly has sent recall letters to its customers and distributors.