Health product recall

Howmedica Revision Instrument System (HRIS) Storage & Sterilization Case and Tray

Last updated

Summary

Product
Howmedica Revision Instrument System (HRIS) Storage & Sterilization Case and Tray
Issue
Medical devices - Sterility Issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Howmedica Revision Instrument System (HRIS) Storage & Sterilization Case and Tray

All lots.

6210-9-900

Issue

Gray revision instruments are single-use, sterile-packaged manual surgical instruments intended for one-time use during hip or knee arthroplasty, or trauma surgeries. The HRIS storage & sterilization case and tray part number 6210-9-900 has dedicated locations that include instrument silhouettes and part number markings that are silkscreen printed on the trays for the instruments. This may lead to the re-use and re-sterilization of these single-use sterile-packaged instruments.

Recall Start Date: May 23, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Stryker Neurovascular

47900 Bayside Parkway, Fremont, California, United States, 94538

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75629

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