Health product recall

Olympus Single Use Electrosurgical Knives

Last updated

Summary

Product
Olympus Single Use Electrosurgical Knives
Issue
Medical devices - Device compatibility
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
Single Use Electrosurgical Knife - Upper Digestive Tract More than 10 numbers, contact manufacturer. KD-640L
Single Use Electrosurgical Knife KD-645 More than 10 numbers, contact manufacturer. KD-645L

Issue

Olympus determined that deterioration of the cutting knife, caused by overheating and burning, can contribute to tip breakage during use. Olympus is also notifying users of the updates to the instructions for use and labeling.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies
Olympus Medical Systems Corp.
2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81439

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