FDA-Device2023-10-18Class II

Medfusion Syringe Pump, Model 3500VX-500, v3, v4, v5, and v6

Smiths Medical ASD Inc.
Hazard

A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor calibration shift is large enough, the pump will display a System Failure Alarm (including Force Sensor BGND Test, Force Sensor Bridge Test, or Force Sensor Test). However, if the calibration shift is not large enough to trigger a System Failure Alarm, the threshold to detect an occlusion may increase, increasing the time to occlusion detection, or the threshold may decrease, leading to false occlusion alarms. Although shifts in the force sensor calibration may occur over time with any device, an increased potential for such shifts has been reported in devices produced before April 2022 due to mechanical interference between parts of the plunger head assembly. Out of an abundance of caution, we are notifying all customers of this potential issue.

Sold states
Worldwide distribution - US Nationwide and the country of Canada.
Affected count
111 pumps
Manufactured in
6000 Nathan Ln N, N/A, Minneapolis, MN, United States
Products
Medfusion Syringe Pump, Model 3500VX-500, v3, v4, v5, and v6

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0077-2024

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