Leica HistoCore Arcadia H, REF: 14039354100 and 14039357258, Paraffin Embedding Station.
FDA Recall Z-2529-2024 · Posted 2024-08-07
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Recalling FirmLEICA BIOSYSTEMS NUSSLOCH GMBH
Recall StatusOpen, Classified
Product CodeIDW
Date Initiated2024-05-10
Product Quantity180 devices
Reason for Recall
An issue with safe usage of the device was identified whereby toxic smoke and internal fire developed resulting from a problem associated with the sealing of the paraffin tank.
Firm Action
The recalling firm issued letters dated 4/30/2024 via email on 5/10/2024. The letter provided the model and serial number of the devices involved, a description of the problem, and immediate actions to be taken. The consignee is to check to see if they have one of the affected instruments and determine whether the Arcadia H is in active use in the facility. If it is, the consignee is to discontinue the use of it immediately and disconnect it from main voltage. If it has not been decommissioned at the time of receipt of the letter, the consignee is to reach out to their sales representative. The sales representative will work with the consignee to determine the disposition of the device according to their local regulations.
The consignee is requested to pass the notification letter to users of the device and to all within their organization who need to know.
The consignee is to confirm receipt of the letter within 5 days by completing the attached acknowledgement form and returning a scanned copy via email.
Root Cause
Device Design
Distribution Pattern
US Nationwide, including government distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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