Health product recall

Nasopore, Otopore, and Hemopore Nasal Dressings

Last updated

Summary

Product
Nasopore, Otopore, and Hemopore Nasal Dressings
Issue
Medical devices - Sterility
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

Nasopore Standard

More than 10 numbers, contact manufacturer.

5400-010-004
5400-010-008

Nasopore Firm

More than 10 numbers, contact manufacturer.

5400-020-004
5400-020-008

Otopore Square Firm

More than 10 numbers, contact manufacturer.

5400-020-100

Otopore Cylinder Standard

More than 10 numbers, contact manufacturer.

5400-010-000

Nasopore FD

More than 10 numbers, contact manufacturer.

5400-020-108

Nasopore Extra Firm

More than 10 numbers, contact manufacturer.

5400-030-008
5400-030-004

Otopore Cylinder Firm

More than 10 numbers, contact manufacturer.

5400-020-000

Hemopore Hemostatic Fragmentable Nasal Dressing

More than 10 numbers, contact manufacturer.

5400-020-208

Issue

There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.

Recall Start Date: February 27, 2025

Additional information

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

Stryker Instruments, A Division Of Stryker Corporation

1941 Stryker Way, Portage, Michigan, United States, 49002

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77087

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