Reported Apr 9, 2025 · Ongoing
Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
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 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
- Lot codes and dates
- 5400-020-008
- UDI-DI07613154340828
- Lot Numbers; 5400-020-008ITL
202210121420230111152023021612202306193220231016322024011532202405151220221013142023011212202303131220230626122023110232202402191420240726312022101414202301131420230314142023062812202311303420240227312024081312202210191420230116152023042413202307243320231207322024030431202408261420230109122023011814202305021220230911122023121532202403193220240828122022101214202301111520230216122023061932202310163220240115322024051512202301101520230213132023051014202309121220231218322024050814
- UDI-DI07613327359428
- Lot Numbers
392 of 392 codes
202210191220230309142023070715202307313220230905122023101012202311083220231206122022102614202303101520230707122023080132202309071220231010142023111314202312063320221107142023032932202307113220230802322023090814202310113320231109322023120714202211081420230426142023071133202308023320230912142023101114202311133220231207122022110914202305011320230711342023080332202309131420231013142023111333202312081420221110142023050312202307113520230807322023091416202310131320231115142023120812202211111420230504122023071232202308073320230915142023101615202311163220231212322022111715202306141420230712332023080932
- 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.
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