Encore Medical, Lp: 28 recalls on record

Recalls filed with 1 agency: FDA (28).

First recall on record: August 15, 2012. Most recent: July 15, 2026.

Risk classification: Class II: 28

Most recent recalls

DateAgencyProduct
July 15, 2026FDABrand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog N…Z-2701-2026
July 15, 2026FDABrand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog N…Z-2700-2026
August 20, 2025FDABrand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16…Z-2286-2025
July 23, 2025FDABrand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11…Z-2126-2025
July 2, 2025FDABrand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm …Z-2008-2025
January 1, 2025FDAEMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705; EMPOWR 3D Knee Tibial Insert…Z-0766-2025
January 10, 2024FDAREF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2Z-0626-2024
January 10, 2024FDAReverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Con…Z-0625-2024
November 15, 2023FDADJO EMPOWR Knee Punch Handle, REF: 801-05-040Z-0258-2024
October 28, 2020FDAAltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03…Z-0117-2021
October 14, 2020FDADJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instr…Z-0060-2021
April 4, 2018FDAAltivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 …Z-1259-2018
April 4, 2018FDAAltivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 54mm, REF 804-07-540 …Z-1260-2018
November 15, 2017FDACobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS…Z-0065-2018
November 15, 2017FDACobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, …Z-0066-2018
November 15, 2017FDACobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, …Z-0067-2018
November 15, 2017FDACobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS…Z-0064-2018
November 1, 2017FDAEMPOWR PS KNEE(TM) e+, REF 343-19-707, SIZE 7, 19mm, QTY 01, GREY, STERILE Product U…Z-0042-2018
November 1, 2017FDAEMPOWR PS KNEE(TM) e+, REF 343-13-708, SIZE 8, 13mm, QTY 01, SKY BLUE, STERILE Produ…Z-0041-2018
September 6, 2017FDAMODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers: REF …Z-3102-2017
July 12, 2017FDA3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3D…Z-2658-2017
March 15, 2017FDATuron Impaction FixtureZ-1412-2017
February 22, 2017FDALIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revisi…Z-1191-2017
December 14, 2016FDAEmpowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, util…Z-0711-2017
May 8, 2013FDA3DKnee e+ Tibial Insert. The insert is used along with the other components that comprise…Z-1213-2013

Questions about this company

How many recalls does Encore Medical, Lp have?
Recalert has 28 U.S. recalls on record for Encore Medical, Lp, published between August 15, 2012 and July 15, 2026.
What was the most recent Encore Medical, Lp recall?
FDA recall Z-2701-2026, published July 15, 2026: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Which agencies have handled Encore Medical, Lp recalls?
Encore Medical, Lp appears as the recalling firm in recalls from: FDA (28).

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