Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Recalled by Stryker Howmedica Osteonics Corp. Due to it was discovered that item 623-10-36I Lot 3Y0KHP,...
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 Howmedica Osteonics Corp. directly.
Affected Products
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
Quantity: 16 units
Why Was This Recalled?
it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined to be unacceptable due to a documentation issue. However the parts were inadvertently shipped to the field.
Where Was This Sold?
This product was distributed to 1 state: WI
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report