The Halo One Thin-Walled Guiding Sheath is a medical device used to introduce or guide the placement of diagnostic and interventional devices into the veins and arteries through an incision in the patient’s leg.
The Food and Drug Administration (FDA) has announced that Bard Peripheral Vascular Inc., the manufacturer of this device, initiated a recall on December 2, 2016. The company issued a Medical Device Recall Notification on January 10, 2017, instructing consignees to stop using and distributing this product and to remove it from the shelves. At Goldberg & Rosen, our dedicated legal team is proud to represent individuals who have been injured by dangerous medical devices.
For more than 40 years, our top Miami personal injury attorneys have been fighting large corporations and insurance companies to obtain justice for our clients. If you or someone you love has been seriously injured by the Halo One Thin-Walled Guiding Sheath, we may be able to assist you in a lawsuit against the manufacturer to recover compensation for the losses you have suffered.





