Stryker recalls Nasopore FD nasal dressings with catalog numbers 5400-020-108 and 5400-020-108ITL due to potential sterility seal breaches. Affected items may have compromised sterility.
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.
Stryker is recalling specific Nasopore FD nasal dressings that could have broken sterility seals, meaning the product might not be sterile. This could lead to infections if used improperly.
The product's blister seal may show a bubble on the packaging, indicating the sterility barrier has been broken. This could allow contamination and increase infection risk during medical use.
Patients using nasal dressings for medical purposes, particularly those with open wounds or infections, are most at risk. The recall affects specific catalog numbers and production lots.
Check for catalog numbers 5400-020-108 or 5400-020-108ITL. Lot numbers include sequences like 2023011317 through 2024080717 for the first catalog number and similar for the second.
Verify the catalog number and lot numbers listed in the recall notice to confirm if your item is affected.
The recall is due to potential blister seal breaches that could compromise sterility, increasing infection risk during medical use.
Check for catalog numbers 5400-020-108 or 5400-020-108ITL with specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Stryker directly for guidance on safe disposal or alternatives.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1476-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1476-2025 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
