PlainRecalls
FDA Devices Moderate Class II Terminated

Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500. Intended for use in critical care areas for the administration of fluids requiring precisely controlled infusion rates.

Reported: April 3, 2013 Initiated: May 14, 2010 #Z-0996-2013

Product Description

Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500. Intended for use in critical care areas for the administration of fluids requiring precisely controlled infusion rates.

Reason for Recall

An issue with the plunger rod seal was identified where the seal had the potential to migrate inside the pump case top during slow rate/ high back pressure infusions.

Details

Recalling Firm
Smiths Medical ASD, Inc.
Units Affected
6
Distribution
Distributed in the state of NH.
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500. Intended for use in critical care areas for the administration of fluids requiring precisely controlled infusion rates.. Recalled by Smiths Medical ASD, Inc.. Units affected: 6.
Why was this product recalled?
An issue with the plunger rod seal was identified where the seal had the potential to migrate inside the pump case top during slow rate/ high back pressure infusions.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 3, 2013. Severity: Moderate. Recall number: Z-0996-2013.