About the Recall:
Voluntary recall of Magic3 Go® Intermittent Silicone Catheters. Our records indicate you may have purchased an affected lot(s) of products between September 22, 2021- March 22, 2023.
Products(s) numbers/models that are affected:
Identify and check the REF and LOT numbers on your Magic3 Go® product(s) customer box label and compare with the table provided at the below link. If you no longer have your customer box, check the REF and LOT on the individual product package you have left. If the REF and LOT numbers in the single package or box match those in the table, the product should not be used and should be discarded.
Compare with the list on the website. Salesforce
Manufacturer Notice/Web Site:
Actions to be taken by customer/Patient:
1-844-8BD- LIFE (1-844-823-5433)
Say “Recall” when prompted
M-F 8am -5pm CT
Email: productcomplaints@bd.com
ACHC Accredited