Public recall detail

Equipro High Frequency Portable (EI-113P)

2023-09-08

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Recall Safety notice
Quick summary

Quick summary: Equipro High Frequency Portable (EI-113P). Date: 2023-09-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Equipro High Frequency Portable (EI-113P). Date: 2023-09-08.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandEquipro
ProductEquipro High Frequency Portable (EI-113P)
IssueMedical devices - Unauthorised device
Recall classType II
IdentificationRA-74253

Affected products

ProductEquipro High Frequency Portable (EI-113P)
LotAll lots.
ModelNot Applicable
Serial numberAll lots.
DescriptionEquipro High Frequency Portable (EI-113P)

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceIndustry
CategoryHealth products - Medical devices - Neurology
CompaniesEquipro 11970 Boul. Albert-Hudon, Montreal, Quebec, Canada, H1G 3K3
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74253
Background{}
CompaniesEquipro 11970 Boul. Albert-Hudon, Montreal, Quebec, Canada, H1G 3K3
AudiencesIndustry
Source updated2023-09-08

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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