Belotero Lidocaine
Brand(s)
Last updated
Summary
Product
Belotero Lidocaine
Issue
Medical devices - Quality issue
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or Serial Number |
Model or catalogue number |
|---|---|---|
Belotero Soft Lidocaine |
256069/1 |
12807 |
Belotero Balance Lidocaine |
326114/1 |
12809 |
Belotero Intense Lidocaine |
556216/1 |
12808 |
Issue
The recall activities are being conducted due to several temperature excursions on inbound shipment to Canada. According, to the assessment by the manufacturer, Anteis S.A, no data is available for Belotero products after repeated freezing and thawing, and an impairment of quality cannot be ruled out.
Recall start date: May 6, 2022.
Additional information
Details
Original published date: 2022-05-19
Alert / recall type
Health product recall
Category
Health product - Medical device - General and plastic surgery
Companies
Anteis S.A.
18, Chemin Des Aulx, Plan-Les-Ouates, Geneva, Switzerland, 1228
Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-64169