Health product recall

Magic3 Go Intermittent Silicone Catheter

Brand(s)
Last updated

Summary

Product
Magic3 Go Intermittent Silicone Catheter
Issue
Medical devices - Sterility Issue
What to do

Review notice & share with customers/users, discontinue sale/usage of inventory & dispose, return reply form. 

Audience
Healthcare
Industry

Affected products

Affected products

Lot or serial number

Model or catalog number

Magic3 Go Intermittent Silicone Catheter

More than 10 numbers, contact manufacturer.

51816
51814
51810
53812G

Issue

BD observed a nonconforming condition where some catheters manufactured had the clear resealing label separating from the product foil pouch, resulting in a possible path into the product packaging that could potentially result in a sterile barrier breach if the delamination reached the foil opening in the foil package.

Recall start date: April 20, 2023

Additional information

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

C.R. Bard, Inc.

8195 Industrial Blvd., Covington, Georgia, United States, 30014

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-73646

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