Reported Apr 9, 2025 · Ongoing

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

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 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
Lot codes and dates
  • 5400-020-004
  • UDI-DI07613154340811
  • Lot Numbers
    • 2022100314
    • 2023013132
    • 2023042514
    • 2023081512
    • 2023110114
    • 2024011514
    • 2024032512
    • 2024082612
    • 2022102514
    • 2023021012
    • 2023050216
    • 2023082811
    • 2023110614
    • 2024011814
    • 2024042914
    • 2023011332
    • 2023021512
    • 2023060214
    • 2023090514
    • 2023111616
    • 2024021213
    • 2024052812
    • 2023012632
    • 2023030814
    • 2023062214
    • 2023091813
    • 2023112112
    • 2024030412
    • 2024073012
    ; 5400-020-004ITL
  • UDI-DI07613327359459
  • Lot Numbers
    • 2022102012
    • 2023011714
    • 2023011714
    • 2023051614
    • 2023081812
    • 2023110914
    • 2024012614
    • 2024030716
    • 2022111514
    • 2023012014
    • 2023012014
    • 2023052314
    • 2023083116
    • 2023112414
    • 2024020714
    • 2024031214
    • 2023010914
    • 2023020214
    • 2023020214
    • 2023062733
    • 2023100914
    • 2023112912
    • 2024021514
    • 2024031814
    • 2023011214
    • 2023051112
    • 2023051112
    • 2023080112
    • 2023101214
    • 2024010912
    • 2024022014
    • 2024032816
    • 2024042314
    • 2024051314
    • 2024052212
    • 2024060512
    • 2024061114

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:55 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.