Stryker Leibinger recalls QUIKFLAP cranium plates with potential packaging compromise after three years. Affected units include specific part numbers for cranial surgery. Contact for details.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Stryker Leibinger is recalling QUIKFLAP cranium plates that may have compromised sterile packaging after three years. This could lead to infection risks during surgery if the packaging fails. Patients using these plates should contact the manufacturer for guidance.
The external sterile packaging may become compromised after three years of use, potentially allowing contamination. This could increase infection risk during surgery if the packaging fails.
Patients who have received QUIKFLAP cranium plates with the listed part numbers for cranial surgery. Those with the specific part numbers are most at risk.
Check for part numbers listed in the recall: 1000100540, 1000100541, 1000101992, and other specific numbers. These plates are used for cranial surgery and were sold with the mentioned part numbers.
Look for the specific part numbers listed in the recall to confirm if your plate is affected.
The external sterile packaging may become compromised after three years, potentially increasing infection risk during surgery.
Contact Stryker Leibinger directly to confirm if your specific part number is affected and get instructions.
The recall does not specify a fix; affected users should contact the manufacturer for guidance.
We’ve drafted a message you can send Stryker Leibinger to request your refund or repair — edit it as you like.
Subject: Recall Z-2906-2018 — Stryker Leibinger Stryker Leibinger Hello, I own a Stryker Leibinger that is covered by recall Z-2906-2018 from Stryker Leibinger. 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.
