PlainRecalls
FDA Devices Moderate Class II Ongoing

Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL

Reported: April 9, 2025 Initiated: February 25, 2025 #Z-1474-2025

Product Description

Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL

Reason for Recall

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.

Details

Recalling Firm
Stryker Corporation
Distribution
US Nationwide distribution.
Location
Portage, MI

Frequently Asked Questions

What product was recalled?
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL. Recalled by Stryker Corporation.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 9, 2025. Severity: Moderate. Recall number: Z-1474-2025.