Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD PERIPHERAL VASCULAR, INC Due to Complaints of sheath separation, kinking, and/or tip damage...

Date: December 2, 2016
Company: BARD PERIPHERAL VASCULAR, INC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact BARD PERIPHERAL VASCULAR, INC directly.

Affected Products

Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Product Usage: The Halo One Thin-Walled Guiding Sheath is designed to perform as both a guiding sheath and introducer sheath. The Halo One Thin-Walled Guiding Sheath is indicated for use in peripheral arterial and venous procedures requiring percutaneous introduction of intravascular devices. The Halo One Thin-Walled Guiding Sheath is NOT indicated for use in the neurovasculature nor the coronary vasculature.

Quantity: 101

Why Was This Recalled?

Complaints of sheath separation, kinking, and/or tip damage during use.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About BARD PERIPHERAL VASCULAR, INC

BARD PERIPHERAL VASCULAR, INC has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report