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No image published for this recall

Intraclude intra-aortic occlusion device (2019-05-22)

Official notice

16 Jul 2019

Last checked

16 Jul 2019

High riskHealth Canada

An official Health Canada notice concerns Intraclude intra-aortic occlusion device (2019-05-22). IntraClude Intra-aortic Occlusion Device (2019-05-22) Published 2019-07-16.

What to do now

The source does not provide specific consumer instructions. Follow the official Health Canada notice for next steps.

Recall number

59786

Official notice

2019-07-16

The hazard

IntraClude Intra-aortic Occlusion Device (2019-05-22)

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

59786

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

59786

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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