Healio

Guiding sheath used in peripheral vascular procedures recalled

Please provide your email address to receive an email when new articles are posted on . The FDA has designated a recall of a sheath used to introduce and/or guide the placement of interventional and ...
TCTMD

Voluntary Recall of Chariot™ Guiding Sheath

MARLBOROUGH, Mass., Boston Scientific has voluntarily recalled the Chariot™ Guiding Sheath globally. These devices are intended for the introduction of interventional devices during peripheral ...
TCTMD

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

Yesterday the US Food and Drug Administration (FDA) announced a Class I recall for the low-profile, thin-walled peripheral guiding sheath known as Halo One. Device manufacturer Bard Peripheral ...
Business Wire

Cook Launches Two New Devices to Improve Ureteral Access; Flexor(R) DL Ureteral Access Sheath and BiWire Nitinol Core Wire Guide Advance Ureteroscopic and Minimally Invasive ...

SPENCER, Ind.--(BUSINESS WIRE)--Aug. 17, 2006--Cook Urological, a division of Cook, the world's largest private medical device company, today announced the availability of the Flexor(R) DL (Dual Lumen ...