Quick summary
Quick summary: TDHistoCyto. Date: 2023-04-04.
Public recall detail
TDHistoCyto
2023-04-04
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: TDHistoCyto. Date: 2023-04-04.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandTechnidata S.A.S.
ProductTDHistoCyto
IssueMedical devices - Performance
Recall classType II
IdentificationRA-73453
Affected products
ProductTDHistoCyto
LotV13.51B V11.71B V13.32S40 V07.01B V11.81B V12.21S50 V11.91B
ModelTD-TDH-01
Serial numberV13.51B V11.71B V13.32S40 V07.01B V11.81B V12.21S50 V11.91B
DescriptionTDHistoCyto
Issue
The recall applies to all versions of TDHistoCyto. Defect: For a specific use case, there is a risk of printing examination slide labels with incorrect information, such as the barcode of the examination request number. Recall start date: March 23, 2023
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesTechnidata S.A.S. 387, Avenue Jean Kuntzmann, Montbonnot Saint Martin, France, 38330
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-73453
Background{}
CompaniesTechnidata S.A.S. 387, Avenue Jean Kuntzmann, Montbonnot Saint Martin, France, 38330
AudiencesHealthcare
Source updated2023-04-04
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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