Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to The device has the potential to release nickel...
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 GmbH directly.
Affected Products
Osteosynthesis Compression Staple EasyClip
Quantity: 121,517 EasyClip devices and 9,561 EasyClip Xpress devices distributed nationwide in US.
Why Was This Recalled?
The device has the potential to release nickel above the acceptable margin of safety in pediatric patients who weigh less than 20 kg (44.09 lbs) when 2 or more implants are used.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker GmbH
Stryker GmbH has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report