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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Z-0326-2018 - DJO EMPOWR KNEE LOCKING TIBIAL PUNCH GUIDE, REF 801-05-042, NON STERILE, Qty 1 For use in orthopedic surgery. 2 01/10/2018 Encore Medical, Lp
Z-0329-2018 - EMPOWR Porous Knee System TIBIAL PUNCH, LARGE, REF 801-05-204, NON STERILE, Qty 1 For use in orthopedic surgery. 2 01/10/2018 Encore Medical, Lp
Z-0328-2018 - EMPOWR Porous Knee System TIBIAL PUNCH, MEDIUM, REF 801-05-203, NON STERILE, Qty 1 For use in orthopedic surgery. 2 01/10/2018 Encore Medical, Lp
Z-0327-2018 - EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery. 2 01/10/2018 Encore Medical, Lp
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