Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet part # 506076, lot 928182 was received...
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 Synvasive Technology Inc directly.
Affected Products
The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage: For use with Stryker System 5, System 4, System 2000 and EDH. A set of three surgical saw blades is used to resect damaged cartilage and/or bone in an orthopedic reconstructive procedure such as a partial knee replacement. The set contains both oscillating blades for tissue resection along a small arc in a left/right or up/down direction, and reciprocating blades for resection back and forth in a single plane.
Quantity: 100 kits
Why Was This Recalled?
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Synvasive Technology Inc
Synvasive Technology Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report