Official recall record
HistoCore PELORIS 3 (ref 77259)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-04-10
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Leica Biosystems has become aware of a leakage issue associated with the tubing in the manifold of the HistoCore PELORIS 3 instrument. Leakage may expose instrument operators and other laboratory personnel to toxic chemicals and pose a slip hazard. Recall start date: April 2, 2025
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.