Health product recall

BiCOAG Hemostasis Probe

Brand(s)
Last updated

Summary

Product
BiCOAG Hemostasis Probe
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

BiCOAG Hemostasis Probe - Fixed Pin Connector

More than 10 numbers, contact manufacturer.

CD-B622LA

BiCOAG Hemostasis Probe - Fixed Pin Connector

More than 10 numbers, contact manufacturer.

CD-B612LA

BiCOAG Hemostasis Probe - Coaxial Connector

More than 10 numbers, contact manufacturer.

CD-B610LA

BiCOAG Hemostasis Probe - Coaxial Connector

More than 10 numbers, contact manufacturer.

CD-B620LA

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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies

Gyrus Acmi, Inc

9600 Louisiana Ave. North, Brooklyn Park, Minnesota, United States, 55445

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82587

Get notified

Receive emails about new and updated recall and safety alerts.

Subscribe