Stryker recalls two nasal dressing products due to potential sterility seal breaches. Affected items have specific catalog numbers and lot dates. Consumers should check packaging for blister seal bubbles to determine if 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.
Stryker is recalling two types of nasal dressings because the sterility seal on the packaging might show a bubble, indicating the seal has been broken. This could mean the product is no longer sterile and unsafe for use.
The blister seal on the packaging is designed to keep the product sterile. If it shows a bubble, the seal has been broken, meaning the product might not be sterile anymore. This could lead to infection if used improperly.
People who own or use the Nasopore 4cm Standard 2PK or Firm 2PK nasal dressings with the specified catalog numbers and lot dates are affected. Those with medical conditions requiring sterile dressings are at higher risk.
Check the packaging for a bubble on the blister seal area. The affected products have catalog numbers 5400-212-004S and 5400-222-004S with specific lot dates: 2024011914 and 2024021212, 2024052813.
Look for a bubble on the blister seal area of the packaging to determine if the sterility seal has been breached.
The recall is happening because the blister seal on the packaging might show a bubble, indicating the sterility seal has been broken, which could mean the product is no longer sterile.
Check the packaging for a bubble on the blister seal area. The affected products have catalog numbers 5400-212-004S and 5400-222-004S with specific lot dates: 2024011914 and 2024021212, 2024052813.
The recall does not require discarding the product; you can check the seal to see if it's safe to use.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1481-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1481-2025 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.
