Public recall detail

Universal Joint Screwdriver

2023-09-18

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Recall Safety notice
Quick summary

Quick summary: Universal Joint Screwdriver. Date: 2023-09-18.

Recommended action

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

Recall details

Quick summary: Universal Joint Screwdriver. Date: 2023-09-18.

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
ProductUniversal Joint Screwdriver
IssueMedical devices - Device compatibility
Recall classType II
IdentificationRA-74302

Affected products

ProductUniversal Joint Screwdriver
Lot1000495789 1000499428 1000491614 1000501513
Model6003-100-110
Serial number1000495789 1000499428 1000491614 1000501513
DescriptionUniversal Joint Screwdriver

Issue

The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material. Recall start date: September 1, 2023

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Neurology
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-74302
Background{}
CompaniesStryker Instruments, A Division Of Stryker Corporation 1941 Stryker Way, Portage, Michigan, United States, 49002
AudiencesGeneral public Healthcare Industry
Source updated2023-09-18

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

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