Stryker recalls Nasopore Standard 4cm nasal dressings with catalog numbers 5400-010-004 and 5400-010-004ITL 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 Nasopore Standard 4cm nasal dressings with specific catalog numbers because the packaging's sterility seal might be broken, risking infection. This is a safety issue for people using these dressings for nasal care.
The packaging has a sterility seal that should stay intact to keep the dressing clean. If this seal shows a bubble, it means the sterility barrier was broken, which could lead to infection if the dressing is used.
People who own or use Nasopore Standard 4cm nasal dressings with catalog numbers 5400-010-004 or 5400-010-004ITL are affected. Those with medical conditions requiring nasal dressings are at slightly higher risk.
Check for catalog numbers 5400-010-004 or 5400-010-004ITL on the packaging. The product is sold with specific lot numbers listed in the recall notice.
Look for a bubble on the sterility seal area of the packaging to determine if the seal has been breached.
The recall does not require discarding the product. Check the sterility seal for bubbles to see if it's safe to use.
If there's no bubble on the seal, the product is likely safe to use as the sterility barrier remains intact.
Check the catalog number on the packaging; the recalled items have catalog numbers 5400-010-004 or 5400-010-004ITL.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1470-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1470-2025 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.
