Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

MaxGuard Extension Set with Injection Site and 0.2 micron filter Recalled by CareFusion 303, Inc. Due to CareFusion is recalling the MaxGuard Extension Set with...

Date: February 20, 2017
Company: CareFusion 303, 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 CareFusion 303, Inc. directly.

Affected Products

MaxGuard Extension Set with Injection Site and 0.2 micron filter, Model No. ME3305

Quantity: 1,200 units

Why Was This Recalled?

CareFusion is recalling the MaxGuard Extension Set with Injection Site and 0.2 micron filter because of reports of separation and/or leakages between the Y-connector and tubing.

Where Was This Sold?

This product was distributed to 2 states: MD, MA

Affected (2 states)Not affected

About CareFusion 303, Inc.

CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.

Related Recalls

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