Stryker recalls Hemopore 2PK nasal/sinus wound dressings with potential sterility seal breaches. Check catalog number 5400-222-208S and lot numbers 2024020221, 2024051720, 2024082321 for affected items.
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 Hemopore 2PK nasal/sinus temporary wound dressings due to a potential sterility seal breach. This could mean the dressing is no longer sterile, risking infection if used.
The product's blister seal may show a bubble on the packaging, indicating the sterility barrier has been broken. This could allow contamination and infection if the dressing is used after the seal breach.
People who own or use Hemopore 2PK nasal/sinus wound dressings with catalog number 5400-222-208S and the listed lot numbers are affected. Those using the product for medical purposes are most at risk.
Check for the catalog number 5400-222-208S on the packaging. Affected items have lot numbers 2024020221, 2024051720, or 2024082321.
Look for a bubble on the blister seal area of the packaging to determine if sterility has been compromised.
The recall states that a bubble indicates a seal breach, but the product may still be safe if no bubble is visible. However, the official notice does not specify if products without bubbles are affected.
The recall does not provide specific action steps for affected products. Check the packaging for the catalog number and lot numbers to confirm if your item is recalled.
Verify by checking the catalog number 5400-222-208S and lot numbers 2024020221, 2024051720, or 2024082321 on the packaging.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1482-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1482-2025 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.
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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.
