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Recall Observatory FDA recall evidence

Device product

Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced during the same time period in which a main board was replaced using replacement main board part numbers G6000361, G6000435, G6001260, G6001560, G6001562 and G6002728.

Z-0653-2022

December 03, 2015

Class II

Product summary

Firm
Smiths Medical ASD Inc.
Event
Event 89144
Status
Ongoing
Classification
Class II
Quantity
38,797 (31,065 pumps and 7,732 boards)
Official record key
device-enforcement:Z-0653-2022

Official wording

Reason: There have been intermittent issues with Supercap POST (power on self-test) and Backup Audible Alarm error codes outside of the pump warranty period. These alarms occur at start up when the pump goes through the self-test. This recall occurred in 2015.

Code information: Medfusion 3500 and 4000 Syringe Infusion Pumps manufactured between April 2012 and June 2015; and Medfusion 3010 and 3010A (and pump models 3500 and 40000 serviced during April 20121 and June 2015 in which a main board was replaced.

Distribution pattern: Distribution US nationwide, including PR, VI, GU, and MP. There was government/military/foreign distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There have been intermittent issues with Supercap POST (power on self-test) and Backup Audible Alarm error codes outside of the pump warranty period. These alarms occur at start up when the pump goes through the self-test. This recall occurred in 2015.