Health product recall

Medline Epidural Catheter

Last updated

Summary

Product
Medline Epidural Catheter
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Epidural Catheter

23GBO701
23GBO702
23GBO700
22FBX111
23GBL403
23FBT886
22FBY472

EPICATH19

Issue

Medline Industries, LP has initiated a recall on convenience kits containing NEXUS™ Connectors A-EP-081 and A-EP-424 from Epimed International Inc. The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position. If the defect is not detected before use, there is a risk of medication leakage. Additionally, if the defect goes unnoticed, there is a risk of the catheter connector disconnecting during use.

Recall start date: October 25, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Obstetrics and gynaecology
Companies
Medline Industries, Lp
Three Lakes Drive, Northfield, Illinois, United States, 60093
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76460

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