Medical DeviceMay 7, 2025
Leica Biosystems Melbourne Pty HistoCore PELORIS 3 recall — FDA Z-1683-2025
There is a leakage issue associated with the tubing in the manifold of the instrument.
Class IIFDA: OngoingLeica Biosystems Melbourne Pty Ltd
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Leica Biosystems Melbourne Pty Ltd as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.