Public recall detail

HistoCore Arcadia H

2024-05-08

medium
Recall Safety notice
Quick summary

Quick summary: HistoCore Arcadia H. Date: 2024-05-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: HistoCore Arcadia H. Date: 2024-05-08.

Official details

Affected product details

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

BrandLeica Biosystems Nussloch GmbH
ProductHistoCore Arcadia H
IssueMedical devices - Performance
Recall classType II
IdentificationRA-75498

Affected products

ProductHistoCore Arcadia H
LotMore than 10 numbers, contact manufacturer.
Model14039354100
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionHistoCore Arcadia H

Issue

As part of the company's post market surveillance, they have identified an issue related to the safe usage of the HistoCore Arcadia H system. The problem is associated with the sealing of the paraffin tank. The process of paraffin solidification in the paraffin tank may lead to the deformation of the tank. This in turn, may cause the sealing of the tank to tear. Subsequent overfilling of the paraffin can cause the excess of melted paraffin to flow into the housing of the HistoCore Arcadia H. The paraffin can then soak into the insulation material. This may cause the saturated insulation material to fall onto the printed circuit board assembly and primary circuit. Because the paraffin-saturated insulation material no longer retains its flame resistance properties, this may lead to the development of toxic smoke and an internal fire in the HistoCore Arcadia H. Instruments manufactured after April 2017 do already have a reinforced tank which avoids any bending. Recall start date: May 2, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare Industry
CategoryHealth products - Medical devices - Pathology
CompaniesLeica Biosystems Nussloch GmbH Heidelberger Street 17-19, Nussloch, Germany, 69226
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75498
Background{}
CompaniesLeica Biosystems Nussloch GmbH Heidelberger Street 17-19, Nussloch, Germany, 69226
AudiencesHealthcare Industry
Source updated2024-05-08

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

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