Stryker recalls QUIKFLAP surgical components due to potential sterile packaging compromise after three years. Affected items include specific part numbers for cranium use. Consumers should check product details and contact Stryker for guidance.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Stryker is recalling QUIKFLAP surgical components that may have compromised sterile packaging after three years. This could lead to infection risks if the packaging is no longer intact.
The sterile packaging may become compromised after three years, potentially allowing contamination. This could lead to infection if the components are used without proper sterility.
Surgical professionals and hospitals using the QUIKFLAP components for cranium procedures. Those with the specific part numbers listed are most at risk.
Check for part numbers 1000225769, 1000239651, or 1000254801 on the packaging. The components are used for cranium procedures and come in specific sizes.
Look for part numbers 1000225769, 1000239651, or 1000254801 on the packaging to confirm if the item is affected.
The sterile packaging may become compromised after three years, potentially leading to contamination risks.
Check for part numbers 1000225769, 1000239651, or 1000254801 on the packaging. These components are used for cranium procedures.
The recall record does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2901-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2901-2018 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.
