Health product recall

Z-Med II-X Catheter

Brand(s)
Last updated

Summary

Product
Z-Med II-X 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 catalog number

Z-Med II-X Catheter

JZX-5322

PDZ733

Issue

These units are being recalled due to them being manufactured with the incorrect balloon. The balloon that was placed on this catheter has a lower rated burst pressure than what the PDZ733 is labeled for. The size and length are correct, but the labeled rated burst pressure is different.

Recall Start Date: October 25, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Numed Inc.

2880 Main Street, Hopkinton, New York, United States, 12965

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-76408

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