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device recall
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Encore Medical, LP device recall (Cls II)

July 9, 2025$EMIupdated 5mo ago
community read0 votes

Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Description: Enovis knee devices are intended for treatment of patients who are candidates for knee arthroplasty per the Indication for use. While total knee replacements are not intended to withstand activity levels and loads of normal healthy bone, they are a means of restoring mobility and reducing pain for many patients. — Reason: Knee implants contain incorrect labeling (size and/or side incorrect) — Status: Ongoing

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same company · ±60 days · 6

  • device recallEncore Medical, LP device recall (Cls II)Jul 9, 2025
  • device 510kEncore Medical L.P. — EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert) (510k cleared)Jul 8, 2025
  • device 510kEncore Medical L.P. — EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones) (510k cleared)Jul 2, 2025
  • device recallEncore Medical, LP device recall (Cls II)Jul 18, 2025
  • device recallEncore Medical, LP device recall (Cls II)Jul 18, 2025
  • device recallEncore Medical, LP device recall (Cls II)Jul 18, 2025

🐶 often sniffed alongside

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  • tagRecall11 co-mentions · 11 sources
  • tagOrthopedics4 co-mentions · 3 sources
  • tagPain4 co-mentions · 3 sources
  • tagOncology1 co-mentions · 1 sources
  • tagRheumatoid Arthritis1 co-mentions · 1 sources

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