Public recall detail

Vanta With Adaptivestim Technology

2023-06-22

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Recall Safety notice
Quick summary

Quick summary: Vanta With Adaptivestim Technology. Date: 2023-06-22.

Recommended action

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

Recall details

Quick summary: Vanta With Adaptivestim Technology. Date: 2023-06-22.

Official details

Affected product details

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

BrandMEDTRONIC INC.
ProductVanta With Adaptivestim Technology
IssueMedical devices - Performance
Recall classType II
IdentificationRA-73868

Affected products

ProductVanta With Adaptivestim Technology
LotMore than 10 numbers, contact manufacturer.
Model977006
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionVanta With Adaptivestim Technology

Issue

Vanta Implantable Neurostimulator (INS) may malfunction after a cardioversion or defrbrillation procedure. The damage/malfunction to the device may no longer allow it to provide therapy or communicate with applications, resulting in a loss of stimulation and the need for an unanticipated surgery to explant/replace the INS. Recall start date : June 6, 2023

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Neurology
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-73868
Background{}
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
AudiencesHealthcare
Source updated2023-06-22

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

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