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# Bard Recalls Halo One Guiding Sheath
- URL: https://www.fdaweb.com/bard-recalls-halo-one-guiding-sheath/
- Published: 2017-01-30T12:00:00.000Z
- Updated: 2026-09-14T22:03:32.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137855

Bard Peripheral Vascular has recalled its Halo One Thin-Walled Guiding Sheath because the sheath body may separate from the sheath hub while removing the device from a patient’s leg. The company also reports that the sheath may kink, and that its tip may become damaged during the procedure, a [recall notice](http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm538831.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery) says. “The affected product may cause other serious adverse health consequences such as internal tears and perforation to arteries or veins, excessive bleeding, and death,” it says.