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.

ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW INTERNATIONAL Inc. Due to Potential for catheter separation or leakage

Date: May 19, 2023
Company: ARROW INTERNATIONAL Inc.
Status: Ongoing
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 ARROW INTERNATIONAL Inc. directly.

Affected Products

ARROW Endurance Extended Dwell Peripheral Catheter System

Quantity: 262,016 units

Why Was This Recalled?

Potential for catheter separation or leakage

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc. has 47 total recalls tracked by RecallDetector.

Related Recalls

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