Public recall detail

Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadra Assura, Assura MP, and Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator (2018-06-01)

medium
Recall Safety notice
Quick summary

Quick summary: Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadra Assura, Assura MP, and Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator (2018-06-01) .

Recommended action

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

Recall details

Quick summary: Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadra Assura, Assura MP, and Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator (2018-06-01) .

Official details

Affected product details

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

Brand

Affected products

DescriptionA. Unify B. Fortify VR C. Fortify DR D. Fortify ST VR E. Fortify ST DR F. Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator G. Fortify Assura DR H. Fortify Assura VR I. Unify Assura J. Quadra Assura K. Quadra Assura MP
Additional official information
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Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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