Stryker Endoscopy Devices
Brand(s)
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 and 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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