Health product recall

Medfusion® Syringe Infusion Pumps

Last updated

Summary

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

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Medfusion® Syringe Infusion Pumps

Contact the manufacturer.

3500
3500-415
3500-500

Medfusion® Model 4000 Syringe Infusion Pump

Contact the manufacturer.

4000-0105-51
4000-0106-01
4000-0101-51

Issue

Smiths Medical identified that certain barrel clamp guides may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded. The affected barrel clamp guide part (mechanism) number is G6000716 and the associated affected lot numbers are P0407365, P0486670 and P0561740. The listed Medfusion® syringe infusion pumps, contain the barrel clamp guide mechanism.

Recall start date: December 28, 2023

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
Recall class
Type II
Identification number
RA-74928

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