Equipro High Frequency Portable (EI-113P)
Brand(s)
Last updated
Summary
Product
Equipro High Frequency Portable (EI-113P)
Issue
Medical devices - Unauthorised device
What to do
Contact the manufacturer if you require additional information.
Audience
Industry
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Equipro High Frequency Portable (EI-113P) |
All lots. |
Not Applicable |
Issue
The Equipro High Frequency Portable EI-113P is non-compliant (not licensed for sale in Canada) as a Class II medical device under Canadian law. Further distribution or use of the remaining product must stop immediately. Please notify any customers to whom you may have sold these units.
Recall Start Date: August 14, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies
Equipro
11970 Boul. Albert-Hudon, Montreal, Quebec, Canada, H1G 3K3
Published by
Health Canada
Audience
Industry
Recall class
Type II
Identification number
RA-74253
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