Public recall detail

Navitracker Kit A : Knee

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Recall Safety notice
Quick summary

Quick summary: Navitracker Kit A : Knee.

Recommended action

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

Recall details

Quick summary: Navitracker Kit A : Knee.

Official details

Affected product details

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

BrandOrthosoft ULC, Dba Zimmer Cas
ProductNavitracker Kit A : Knee
IssueMedical devices - Increased risk or new adverse events
Recall classType II
IdentificationRA-63858

Affected products

ProductNavitracker Kit A : Knee
Lot110221A1
Model20-8000-000-07
Serial number110221A1
DescriptionNavitracker Kit A : Knee

Issue

Zimmer Biomet is conducting a medical device recall for one lot of the Navitracker Kit A : Knee product, which is a nonpatient contacting device used during computer and robotic assisted surgeries. The product in scope was released for distribution without passing sterilization results. this could potentially lead to insufficient sterility of the product, which may lead to the risks identified. Recall start date: Jan 13, 2022

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - Neurology
CompaniesOrthosoft Ulc, Dba Zimmer Cas 75 Queen Street, Montreal, Quebec Canada, H3C 2N6
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63858
Background{}
CompaniesOrthosoft Ulc, Dba Zimmer Cas 75 Queen Street, Montreal, Quebec Canada, H3C 2N6
AudiencesGeneral public Health professionals Hospitals
Source updated2022-01-24

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

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