Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DJO EMPOWR KNEE LOCKING TIBIAL PUNCH GUIDE Recalled by Encore Medical, Lp Due to The Locking Punch Guide was not sufficiently guiding...
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
DJO EMPOWR KNEE LOCKING TIBIAL PUNCH GUIDE, REF 801-05-042, NON STERILE, Qty 1 For use in orthopedic surgery.
Quantity: 2 units
Why Was This Recalled?
The Locking Punch Guide was not sufficiently guiding the large press fit punch, causing the implant to be placed 2-3mm more posterior than intended.
Where Was This Sold?
One medical device distributor in California.
About Encore Medical, Lp
Encore Medical, Lp has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report