Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EMPOWR Partial Knee Peg Drill Recalled by Encore Medical, LP Due to There have been issues experienced with the peg...
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 Encore Medical, LP directly.
Affected Products
EMPOWR Partial Knee Peg Drill; Model: 800-06-008.
Quantity: 28 units
Why Was This Recalled?
There have been issues experienced with the peg preparation steps, specifically drilling of the Femoral posterior peg. Upon drilling, the shaft portion of the drill may bind within the Posterior Peg drill guide. The extended length of the drill guide and tight tolerances to ensure accurate preparation seem to be contributing to this situation. There is a potential of a delay in surgery if this issue were to recur.
Where Was This Sold?
This product was distributed to 12 states: AZ, CA, FL, GA, IL, IN, MI, MN, NY, TX, VA, WA
About Encore Medical, LP
Encore Medical, LP has 54 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report