Quick summary
Quick summary: Evangeline Biostimulator. Date: 2025-01-02.
Public recall detail
Evangeline Biostimulator
2025-01-02
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Evangeline Biostimulator. Date: 2025-01-02.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandPallianera Pharma Inc
ProductEvangeline Biostimulator
IssueMedical devices - Unauthorised device
Recall classType II
IdentificationRA-76790
Affected products
ProductEvangeline Biostimulator
LotAll lots.
ModelPLN-001
Serial numberAll lots.
DescriptionEvangeline Biostimulator
Issue
Due to improper packing and labelling information Pallianera Pharma has manufactured and distributed unlicenced medical devices. Recall Start Date: December 5, 2024
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceIndustry
CategoryHealth products - Medical devices
CompaniesPallianera Pharma Inc 88 Bloor Street East, Toronto, Ontario, Canada, M4W 3G9
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76790
Background{}
CompaniesPallianera Pharma Inc 88 Bloor Street East, Toronto, Ontario, Canada, M4W 3G9
AudiencesIndustry
Source updated2025-01-02
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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Answers based on the official recall notice.
Product images
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