Health product recall

Endoscopy Trocar

Brand(s)
Aesculap AG
Last updated

Summary

Product
Endoscopy Trocar
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

Endoscopy Trocar

More than 10 numbers, contact manufacturer.

EK083P

Endoscopy Trocar

More than 10 numbers, contact manufacturer.

EK086P

Endoscopy Trocar Reducing Converter

More than 10 numbers, contact manufacturer.

EK087P

Issue

Aesculap AG identified through investigations of complaints that the yellow sealing component of the affected reusable trocar systems 10mm and 12mm exhibits uneven edges with visible silicone fragments.

Additional information

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

Aesculap AG

Am Aesculap Platz, Tuttlingen, Germany, 78532

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-78173

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Date modified: