Public recall detail

Evolut Pro+ Transcatheter Aortic Valve

2022-12-13

medium
Recall Safety notice
Quick summary

Quick summary: Evolut Pro+ Transcatheter Aortic Valve. Date: 2022-12-13.

Recommended action

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

Recall details

Quick summary: Evolut Pro+ Transcatheter Aortic Valve. Date: 2022-12-13.

Official details

Affected product details

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

BrandMedtronic Corevalve Llc
ProductEvolut Pro+ Transcatheter Aortic Valve
IssueMedical devices - Labelling and packaging
Recall classType I
IdentificationRA-72354

Affected products

ProductEvolut Pro+ Transcatheter Aortic Valve
LotMore than 10 numbers, contact manufacturer.
ModelEVPROPLUS-34
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionEvolut Pro+ Transcatheter Aortic Valve

Issue

Infolding is a known phenomenon and occurs when the valve frame folds inward along a vertical line away from the valve inflow and appears as a seam in the frame or as overlapping frame cells on radiographic imaging. Infolding is different and distinct from valve under expansion and may be seen intraprocedurally at deployment or during recapturing of a valve. Although the overall incidence of frame infolding is low in Pro+ TAVs, the Pro+ 34mm TAV has been associated with higher rates of infolding than other Pro+ sizes. From commercial launch on 01-October-2019 to 31-August-2022, the Pro+ 34mm TAV infolding rate was 2.93% of this incidence rate, 0.32% resulted in serious adverse events, including two (2) deaths. Other serious adverse events may include unplanned surgery/intervention, such as surgical explant / valve replacement /aortic repair or implantation of a transcatheter valve within the initial valve (tav in tav), aorticpage 2 of 4 regurgitation/insufficiency, paravalvular leak, hypotension, congestive heart failure, and aortic dissection. In accordance with Medtronic's commitment to patient safety, we will be updating the instructions for use (IFU) with respect to: • detection of infold • removal of an infolded valve and replacement with a new system • pre-dilatation guidance Recall start date: December 5, 2022

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesMedtronic Corevalve Llc 1851 East Deere Avenue, Santa Ana, California, United States, 92705
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-72354
Background{}
CompaniesMedtronic Corevalve Llc 1851 East Deere Avenue, Santa Ana, California, United States, 92705
AudiencesHealthcare
Source updated2022-12-13

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

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