Health product recall

Stryker Endoscopy Devices

Last updated

Summary

Product
Stryker Endoscopy Devices
Issue
Medical devices - Device compatibility
What to do

Contac the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Produits touchés

Numéro de série ou de lot

Numéro de modèle ou de catalogue

Sdc3 Hd Information Management System

16F013664
18F576924
17I534954
16D029604
18G546604

0240060100

Pneumoclear

2106CE0052
2111CE0939
2208CE1322
1704CE0558
2111CE0937
2010CE0366
2203CE0032

0620050000

1688 4k Camera Control Unit With Advanced Imaging Modality

20J536204
19K514104

1688010000

Issue

Smart tags (bluetooth powered tracking devices) were placed in multiple loaner devices manufactured by Stryker Endoscopy without undergoing verification and validation testing to ensure no adverse effect on product functionality.

Recall start date: August 2, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology & Urology
Health products - Medical devices - General hospital and personal use
Companies
W.O.M. World Of Medicine Gmbh
Salzufer 8, Berlin, Berlin, Germany, 10587
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74137

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