Public recall detail

Alphenix INFX-8000C

2023-05-19

medium
Recall Safety notice
Quick summary

Quick summary: Alphenix INFX-8000C. Date: 2023-05-19.

Recommended action

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

Recall details

Quick summary: Alphenix INFX-8000C. Date: 2023-05-19.

Official details

Affected product details

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

BrandCanon Medical Systems Corporation
ProductAlphenix INFX-8000C
IssueMedical devices - Performance
Recall classType II
IdentificationRA-73688

Affected products

ProductAlphenix INFX-8000C
LotPFC2237004
ModelINFX-8000C/PF
Serial numberPFC2237004
DescriptionAlphenix INFX-8000C

Issue

It has been found that the c-arm and table may not be able to operate because the soldering on the tableside console printed wiring board was not done properly. Recall start date: May 8, 2023

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesCanon Medical Systems Corporation 1385, Shimoishigami, Otawara-Shi, Tochigi-Ken, Japan, 324-8550
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-73688
Background{}
CompaniesCanon Medical Systems Corporation 1385, Shimoishigami, Otawara-Shi, Tochigi-Ken, Japan, 324-8550
AudiencesHealthcare
Source updated2023-05-19

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

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