Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit Recalled by Stryker Howmedica Osteonics Corp. Due to Stryker received reports from the field of the...
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
Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France Made in USA non-sterile
Quantity: 211 units
Why Was This Recalled?
Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle.
Where Was This Sold?
This product was distributed to 6 states: IL, MA, MN, ND, OR, PA
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