Public recall detail

Stryker Instruments Break-away Femoral Nozzle

2023-08-16

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Recall Safety notice
Quick summary

Quick summary: Stryker Instruments Break-away Femoral Nozzle. Date: 2023-08-16.

Recommended action

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

Recall details

Quick summary: Stryker Instruments Break-away Femoral Nozzle. Date: 2023-08-16.

Official details

Affected product details

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

BrandStryker Instruments, A Division Of Stryker Corporation
ProductStryker Instruments Break-away Femoral Nozzle
IssueMedical devices - Performance
Recall classType II
IdentificationRA-74135

Affected products

ProductAdvanced Cement Mixing Bowl, Empty Cement Cartridge And Nozzle
LotMore than 10 numbers, contact manufacturer.
Model0306-563-000
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAdvanced Cement Mixing Bowl, Empty Cement Cartridge And Nozzle
ProductHigh Vacuum Cement Injection System And Instrumentations
Lot22314012 22336012
Model0206-512-000
Serial number22314012 22336012
DescriptionHigh Vacuum Cement Injection System And Instrumentations
ProductAdvanced Cement Mixing Bowl, Empty Cement Cartridge, Nozzle And Pressurizer
Lot22314012 22349012
Model0306-573-000
Serial number22314012 22349012
DescriptionAdvanced Cement Mixing Bowl, Empty Cement Cartridge, Nozzle And Pressurizer

Issue

There is potential for the break-away femoral nozzle, the applicator tip connecting the cement cartridge, to disassemble from the system during use. Recall start date: August 1, 2023

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Orthopaedics
CompaniesStryker Instruments, A Division Of Stryker Corporation 1941 Stryker Way, Portage, Michigan, United States, 49002
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74135
Background{}
CompaniesStryker Instruments, A Division Of Stryker Corporation 1941 Stryker Way, Portage, Michigan, United States, 49002
AudiencesHealthcare
Source updated2023-08-16

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

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