Public recall detail

BiCOAG Hemostasis Probe

2026-09-02

medium
Health products Health product recall
Quick summary

Quick summary: BiCOAG Hemostasis Probe. Reason: Health product recall. Category: Health products. Date: 2026-09-02.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: BiCOAG Hemostasis Probe. Reason: Health product recall. Category: Health products. Date: 2026-09-02.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandGyrus Acmi, Inc
ProductBiCOAG Hemostasis Probe
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82587

Affected products

ProductBiCOAG Hemostasis Probe - Fixed Pin Connector
LotMore than 10 numbers, contact manufacturer.
ModelCD-B622LA
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBiCOAG Hemostasis Probe - Fixed Pin Connector
ProductBiCOAG Hemostasis Probe - Fixed Pin Connector
LotMore than 10 numbers, contact manufacturer.
ModelCD-B612LA
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBiCOAG Hemostasis Probe - Fixed Pin Connector
ProductBiCOAG Hemostasis Probe - Coaxial Connector
LotMore than 10 numbers, contact manufacturer.
ModelCD-B610LA
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBiCOAG Hemostasis Probe - Coaxial Connector
ProductBiCOAG Hemostasis Probe - Coaxial Connector
LotMore than 10 numbers, contact manufacturer.
ModelCD-B620LA
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBiCOAG Hemostasis Probe - Coaxial Connector

Issue

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 you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesGyrus Acmi, Inc 9600 Louisiana Ave. North, Brooklyn Park, Minnesota, United States, 55445
Recall date2026-08-18
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82587
Background{}
CompaniesGyrus Acmi, Inc 9600 Louisiana Ave. North, Brooklyn Park, Minnesota, United States, 55445
AudiencesHealthcare
Source updated2026-09-02

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

Official source Monitor products Back to recalls

Starting...

Related recalls

Similar recalls and safety notices.

Loading related recalls...