Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year term, there is a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Leibinger GmbH & Co. KG directly.
Affected Products
QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher).
Quantity: 22,831 total
Why Was This Recalled?
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Where Was This Sold?
This product was distributed to 4 states: AZ, FL, NH, OH
About Stryker Leibinger GmbH & Co. KG
Stryker Leibinger GmbH & Co. KG has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report