Public recall detail

Cerebase Da Guide Sheath

2024-02-16

medium
Recall Safety notice
Quick summary

Quick summary: Cerebase Da Guide Sheath. Date: 2024-02-16.

Recommended action

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

Recall details

Quick summary: Cerebase Da Guide Sheath. Date: 2024-02-16.

Official details

Affected product details

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

BrandMedos International Sarl
ProductCerebase Da Guide Sheath
IssueMedical devices - Performance
Recall classType II
IdentificationRA-75080

Affected products

ProductCerebase Da Guide Sheath
LotMore than 10 numbers, contact manufacturer.
ModelGS9080SD GS9095SD GS9090SD
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionCerebase Da Guide Sheath

Issue

Medos has received an increase in complaints for Cerebase Da Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in extreme rare occasions it may result in embolism. Recall start date: February 7, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesMedos International Sarl Chemin-Blanc 38, Le Locle, Switzerland, 2400
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75080
Background{}
CompaniesMedos International Sarl Chemin-Blanc 38, Le Locle, Switzerland, 2400
AudiencesHealthcare
Source updated2024-02-16

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

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