Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Instrument Tray Recalled by Stryker GmbH Due to The faceplates may incorrectly identify the T2 Basic...
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
Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Quantity: 17 units
Why Was This Recalled?
The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.
Where Was This Sold?
In the countries of Canada and Korea
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