Health product recall

Medfusion Syringe Infusion Pumps

Last updated

Summary

Product
Medfusion Syringe Infusion Pumps
Issue
Medical devices - Performance
What to do

Contact JENI PANDYA at 514‐905‐2012 (JENI.PANDYA@ICUMED.COM) and SHUI YEE KUAN at 514‐905‐2645
 

Audience
Healthcare
Industry

Affected products

Affected products Lot or serial number Model or catalog number
Medfusion Syringe Infusion Pumps Not applicable. 3500G 3500SD-500 3500VX-500 3500-402 3500E 3500VX-415 3500 3500-415 3500VX-414 3500-306 3500-414 3500-500 3500SD 3500VX 3500ZE 3500BC 3500VX-306
Medfusion Model 4000 Syringe Infusion Pump Not applicable. 4000-0101-249 4000-0101-50 4000-0105-51 4000-0105-249 4000-0105-78 4000-0106-00 4000-0106-01 4000-0101-78 4000-0100-50 4000-0106-231 4000-0101-51 4000-0105-50

Issue

Smiths Medical is issuing this letter to notify customers not to use Cardinal Health branded Monoject syringes with Medfusion 3500 and 4000 Syringe Pumps. On September 20, 2023, Cardinal Health issued a medical device product correction for the Cardinal Health branded Monoject Luer-Lock Tip Syringes due to demonstrated recognition and compatibility issues with syringe infusion pumps due to changes made to the dimensions of the syringes. As a result, Cardinal Health recommends that these syringes not be used on syringe infusion pumps.

Recall Start Date: February 29, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Smiths Medical Asd, Inc.

6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-75242

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