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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