Class II — Potential Health Hazard

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

Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to Certain Barrel Clamp Guides may contain a ridge...

Date: April 13, 2018
Company: Smiths Medical ASD 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 Smiths Medical ASD Inc. directly.

Affected Products

Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism

Quantity: 276 units

Why Was This Recalled?

Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.

Where Was This Sold?

This product was distributed to 26 states: AL, AZ, CA, FL, IL, IN, KS, KY, LA, MD, MA, MI, MN, MO, NJ, NM, NY, OH, OK, PA, TN, TX, UT, VA, WA, DC

Affected (26 states)Not affected

About Smiths Medical ASD Inc.

Smiths Medical ASD Inc. has 169 total recalls tracked by RecallDetector.

Related Recalls

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