Official recall record
BiCOAG Hemostasis Probe
- Issuing authority
- Health Canada
- Alert date
- 2026-09-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Olympus determined that the affected products may have been manufactured without the designated amount of adhesive to the rear of the device's ceramic tip, which may result in detachment of the ceramic tip. Customers should immediately discontinue using the BiCOAG Hemostasis Probe products and contact Olympus to return the product.
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 — official record →
Record last checked against the registry on 2026-09-12.
Record last checked against the registry on 2026-09-12.
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