Public recall detail

Belotero Lidocaine

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Recall Safety notice
Quick summary

Quick summary: Belotero Lidocaine.

Recommended action

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Recall details

Quick summary: Belotero Lidocaine.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandAnteis S.A.
ProductBelotero Lidocaine
IssueMedical devices - Quality
Recall classType II
IdentificationRA-64169

Affected products

ProductBelotero Soft Lidocaine
Lot256069/1
Model12807
Serial number256069/1
DescriptionBelotero Soft Lidocaine
ProductBelotero Balance Lidocaine
Lot326114/1
Model12809
Serial number326114/1
DescriptionBelotero Balance Lidocaine
ProductBelotero Intense Lidocaine
Lot556216/1 556231/1
Model12808
Serial number556216/1 556231/1
DescriptionBelotero Intense Lidocaine

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.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesAnteis S.A. 18, Chemin Des Aulx, Plan-Les-Ouates, Geneva, Switzerland, 1228
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64169
Background{}
CompaniesAnteis S.A. 18, Chemin Des Aulx, Plan-Les-Ouates, Geneva, Switzerland, 1228
AudiencesGeneral public Health professionals Hospitals
Source updated2022-05-16

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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