Reported Apr 9, 2025 · Ongoing

Nasopore Ex Firm 8cm fragmentable nasal dressing, Catalog Number 5400-030-008 and Nasopore Forte plus 8cm Catalog…

Stryker Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker Corporation · 1941 Stryker Way · Portage, MI · 49002-9711

Is this the product you have?

  • Nasopore Ex Firm 8cm fragmentable nasal dressing, Catalog Number 5400-030-008 and Nasopore Forte plus 8cm Catalog Number 5400-030-008ITL
Lot codes and dates
  • 5400-030-008
  • UDI-DI07613154340842
  • Lot Numbers
    • 2023012515
    • 2023012715
    • 2023022012
    • 2023050814
    • 2023072632
    • 2023102312
    • 2023102612
    • 2024032514
    2024040212; 5400-030-008ITL
  • UDI-DI07613327359473
  • Lot Numbers
    • 2022092714
    • 2023020633
    • 2023032433
    • 2023050915
    • 2023052514
    • 2023062216
    • 2023082814
    • 2023101112
    • 2024031812
    • 2022092914
    • 2023020814
    • 2023032814
    • 2023051114
    • 2023053115
    • 2023062032
    • 2023090618
    • 2023101714
    • 2024042212
    • 2022101332
    • 2023020915
    • 2023033016
    • 2023051215
    • 2023060914
    • 2023082215
    • 2023100312
    • 2023102014
    • 2024042312
    • 2022121932
    • 2023021416
    • 2023050115
    • 2023052214
    • 2023061412
    • 2023082312
    • 2023100412
    • 2024030414
    • 2024061814
    • 2022122032
    • 2023022032
    • 2023050515
    • 2023052412
    • 2023061514
    • 2023082514
    • 2023100912
    • 2024030512
    • 2024062814
Amount recalled
182,344 total units

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Where it was sold

  • Nationwide

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new packaged foods recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:36 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.