Recall
FDAHealthJuly 9, 2025

Encore Medical, LP — Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 342-16-707 Product Description: Enovis knee devices are int

⚠️ Knee implants contain incorrect labeling (size and/or side incorrect)

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
July 9, 2025

US Nationwide distribution in the states of AL, AZ, CA, CO, FL, IA, IL, IN, KS, LA, NY, TN, TX.

What's affected?

Product
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 342-16-707 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.
Lot code
Item:

Additional details

Lot Code: Item: 342-16-707 GTIN: 00888912167642 Lot: 161T1053, 161T1054

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 40 implants.

View original FDA notice →

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