Fotofinder ATBM Master
Brand(s)
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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