Health product recall

HistoCore Arcadia H

Last updated

Summary

Product
HistoCore Arcadia H
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare
Industry

Affected products

Affected products

Lot or serial number

Model or catalog number

HistoCore Arcadia H

More than 10 numbers, contact manufacturer.

14039354100

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Pathology
Companies

Leica Biosystems Nussloch GmbH

Heidelberger Street 17-19, Nussloch, Germany, 69226

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-75498

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