Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a different inner diameter than...
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
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S
Quantity: 52
Why Was This Recalled?
The devices have a different inner diameter than the diameter specified on the outer box label.
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