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 |
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: 2023-05-09
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