Health product recall

Medfusion Syringe Infusion Pumps

Last updated

Summary

Product
Medfusion Syringe Infusion Pumps
Issue
Medical devices - Performance issue
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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