OFFICIAL-SOURCE RECALL · CANADA
BiCOAG Hemostasis Probe Recall: Olympus determined that the affected products may
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- BiCOAG Hemostasis Probe
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
Hazard
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.
Official recall notice
BiCOAG Hemostasis Probe
Agency: Health Canada
Official publication date: September 2, 2026
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
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