Health product recall

Fotofinder ATBM Master

Last updated

Summary

Product
Fotofinder ATBM Master
Issue
Medical devices - Unauthorised device
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
Fotofinder ATBM Master Not applicable. Not applicable.

Issue

Following a medical device reclassification from MDD of the device , the company Fotofinfer System, Inc  has decided to cease selling the Fotofinder ATBM Master in Canada and notify customers. 

Recall start date: October 21, 2022

Additional information

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

Fotofinder Systems, Inc

7100 Columbia Gateway Dr. Suite 120, Columbia, Maryland, United States, 21046

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72173

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