Encore Medical, LP recalls
Every recall we track for Encore Medical, LP — 80 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Encore Medical, LP more than tripled in 2025 (14, up from 2 in 2024).
All FDA recall records for Encore Medical, LP since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 2 | 9 | 2 | 13 |
| 2018 | 0 | 3 | 3 | 5 | 11 |
| 2019 | 0 | 1 | 1 | 0 | 2 |
| 2020 | 0 | 5 | 2 | 0 | 7 |
| 2021 | 0 | 0 | 4 | 0 | 4 |
| 2022 | 0 | 0 | 4 | 0 | 4 |
| 2023 | 0 | 2 | 14 | 0 | 16 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 4 | 10 | 0 | 14 |
| 2026 (to date) | 0 | 0 | 7 | 0 | 7 |
Most common reasons for Encore Medical, LP recalls
What to do if you have a recalled Encore Medical, LP product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Encore Medical, LP recalls
44 shown- Lower riskMedical device
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product
Encore Medical recalls EMPOWR 3D KNEE INS 11L 14MM VE (model 342-19-703) due to incorrect product size packaging. This may cause confusion during knee surgery. No action needed as it's a packaging error, not a safety hazard.
Encore MedicalFeb 16, 2026 - Lower riskMedical device
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus
Encore Medical recalls RSP Humeral Socket Inserts with incorrect labeling that may cause confusion during surgery. Affected models include 509-00-432 (Lot 385P1263).
Encore MedicalJan 15, 2026 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705
Encore Medical recalls EMPOWR 3D Knee Tibial Insert 5R 14MM (REF: 342-14-705) due to packaging discrepancies that may cause surgical delays. Affected units have specific lot numbers and expiration dates.
Encore MedicalJan 5, 2026 - Use cautionMedical device
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number:
DJO SURGICAL recalls 6.5mm ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL (model 804-06-312) due to potential binding during use. Affected units may kick or bind, causing injury. Contact DJO SURGICAL for details.
DJO SURGICALJul 18, 2025 - Lower riskMedical device
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number:
Encore Medical recalls EMPOWR 3D Knee TIBIAL INSERT E-PLUS (model 341-16-704) due to incorrect labeling of size and side. This may lead to improper implant fitting.
Encore MedicalJul 9, 2025 - Lower riskMedical device
Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40
Encore Medical recalls EMPOWR Dual Mobility hip implants (model 952-28-40E) due to incorrect tibial inserts being packaged. Affected patients should contact the manufacturer for details.
EMPOWRJun 12, 2025 - Lower riskMedical device
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 12MM, VE Model/Catalog
Encore Medical recalls EMPOWR 3D knee tibial inserts due to packaging errors that may lead to incorrect product selection and revision surgery.
Encore MedicalJun 2, 2025 - Lower riskMedical device
Encore Medical, LP recalls Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number:
Encore Medical recalls ALTIVATE REVERSE Torx Peripheral screws (model 506-04-126) due to incorrect size labeling on packaging. This may cause improper use in shoulder replacements.
Encore MedicalMay 28, 2025 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705; EMPOWR 3D Knee Tibial Insert, 3R 14MM, VE, REF: 342-14-703
Encore Medical recalls two knee tibial inserts that may be mixed up, causing delays in getting the correct surgical product. Affected items have specific model numbers and lot codes.
Encore MedicalDec 18, 2024 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706
Encore Medical recalls EMPOWR 3D Knee Tibial Insert 6R 10MM model due to potential surgical delay from an acetabular system in the package.
Encore MedicalDec 10, 2024 - Lower riskMedical device
Encore Medical, LP recalls DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated SIZE 8 Left 3D MATRIX COATED REF 243-01-108 DJO
DJO recalls a specific porous knee surgical system due to incorrect product packaging. Affected units have model numbers 243-01-108 and 353-03-108. Consumers should contact DJO for details.
DJONov 10, 2023 - Lower riskMedical device
Encore Medical, LP recalls Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
Encore Medical recalls Reverse Shoulder System e+ (REF 509-01-032) due to mislabeling. Affected units have specific UDI and lot numbers. No action needed per recall details.
Encore MedicalOct 5, 2023 - Use cautionMedical device
Encore Medical, LP recalls DJO EMPOWR Knee Punch Handle, REF: 801-05-040
Encore Medical recalls DJO EMPOWR Knee Punch Handle (REF 801-05-040) due to breaking during surgery, risking surgical disruption. Affected units include specific lot numbers.
Encore MedicalSep 29, 2023 - Lower riskMedical device
Encore Medical, LP recalls RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.
Encore Medical recalls RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm (REF: 509-01-436) due to potential wrong device for surgery, causing delays. Check UDI-DI: 00888912144667, Lot: 390P1157.
Encore MedicalSep 25, 2023 - Use cautionMedical device
Encore Medical, LP recalls RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
DJO Surgical recalls RSP Glenoid Baseplate model 508-32-204 due to coating hex not engaging with standard tools, risking improper installation.
DJO SurgicalSep 6, 2023 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System, Liner, 10¿ Hooded, HXe+, 40H, REF: 942-01-40H
Encore Medical recalls EMPOWR Acetabular System (REF 942-01-40H) due to swapped hip/knee parts in packaging. Surgeons may use incorrect components during surgery. Affected units have specific UDI-DI and lot numbers.
Encore MedicalAug 22, 2023 - Lower riskMedical device
Encore Medical, LP recalls REVERSE PROSTHESIS SHOULDER SYSTEM, SCREW, LOCKING BONE, RSP, 5mmX30mm long, REF: 506-03-130
Encore Medical recalls reverse shoulder prosthesis screws that may be 3.5mm instead of 5mm, risking surgical delays and poor fixation. Affected units have specific UDI-DI and lot numbers.
Encore MedicalAug 22, 2023 - Lower riskMedical device
Encore Medical, LP recalls DJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106
DJO Surgical recalls Empowr Knee and Universal Tibia Baseplate models due to unsterilized components that may cause infection after implant. Affected units have specific UDI-DI/Lot/Expiration codes.
DJO SurgicalAug 4, 2023 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Porous Knee Patella Over Drill, REF: 802-05-104; EMPOWR Knee Patella Drill, REF: 802-05-108
Encore Medical recalls two EMPOWR knee drills due to incorrect diameter markings that could cause implant loosening or bone fractures during surgery.
Encore MedicalFeb 28, 2023 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706; EMPOWR VVC KNEE TIBIAL INSERT, SIZE 7, 22MM, REF:
Encore Medical recalls knee tibial inserts with incorrect size labeling that could lead to surgical delays or wrong pin sizes during surgery. Affected products include specific sizes and reference numbers.
Encore MedicalDec 22, 2022 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant component.
Encore Medical recalls EMPOWR hip liner implants due to potential mix-ups in surgical components, which could delay hip surgeries. Affected patients should contact the manufacturer for details.
Encore MedicalAug 12, 2022 - Lower riskMedical device
Encore Medical, LP recalls DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert, REF: 342-10-708
Encore Medical recalls DJO EMPOWR 3D Right Knee 10mm Tibial Insert (REF: 342-1:0708) due to possible mispackaged left size 4 insert that could leave debris in the joint.
Encore MedicalMay 5, 2022 - Lower riskMedical device
Encore Medical, LP recalls AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000,
Encore Medical recalls AltiVate Anatomic Shoulder System parts due to humeral stem failing to mate with broach handles, potentially causing procedure delays or revision surgery.
Encore MedicalJun 28, 2021 - Lower riskMedical device
Encore Medical, LP recalls DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI:
DJO Surgical recalls EMPOWR 3D Knee Tibial Insert e-plus models with packaging mixup risk. Incorrect size knee prostheses may be shipped. Check your product label for serial number and size.
DJO SurgicalMay 12, 2021 - Lower riskMedical device
Encore Medical, LP recalls DJO EMPOWR KNEE Femoral Sizer
Encore Medical recalls DJO EMPOWR KNE: Incorrect assembly causes windows to face opposite direction. Check model 800-05-034 lot 326336L02 for affected units.
Encore MedicalFeb 5, 2021 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System *** EMPOWR Acetabular Cup, Cluster Hole, 54G *** Size 54G 54 mm Dia./Cluster Hole Alpha Code G
Encore Medical recalls EMPOWR Acetabular Cup (Size 54G) due to incomplete machining causing a protruding peg that may lead to improper seating. Affected patients should contact for details.
Encore MedicalSep 9, 2020 - Lower riskMedical device
Encore Medical, LP recalls AltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03-044 - Product Usage: Per IFU,
Encore Medical recalls AltiVate Reverse Small Socket Insert (Part 509-03-044) due to mislabeling that may delay or stop surgery. Affected units sold with lot number 964W100:1000.
Encore MedicalAug 31, 2020 - Use cautionMedical device
Encore Medical, LP recalls RSP Standard HUMERAL SOCKET INSERT, 44MM, HXe-Plus, Part No. 509-00-044
Encore Medical recalls RSP Standard Humerus Socket Insert (44mm) due to possible size mismatch with patient labels, risking incorrect implant and surgery complications.
Encore MedicalAug 7, 2020 - Use cautionMedical device
Encore Medical, LP recalls DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous
DJO recalls EMPOWR Tibial Knee Punch Handles with part numbers 801-05-040 and 801-05-018 due to potential pin loosening that could leave debris in the joint. Affected units have specific lot numbers.
DJOAug 3, 2020 - Use cautionMedical device
Encore Medical, LP recalls EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Encore Medical recalls EMPOWR Partial Knee Peg Drill Guide model 800-06-007 due to potential drilling issues that may delay surgery. All units are affected.
Encore MedicalJun 19, 2020 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System, Non-Sterile, Model Numbers 803-15-023 803-15-026 803-15-027 803-15-028 803-15-029 803-15-030
Encore Medical recalls EMPOWR Acetabular System models 803-15-023 to 803-15-030 due to fracturing impactor balls that could cause joint debris. Affected patients should contact manufacturer for details.
Encore MedicalOct 22, 2019 - Use cautionMedical device
Encore Medical, Lp recalls EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Encore Medical recalls EMPOWR Locking Femoral Impactor parts due to breakage risks and potential misalignment causing surgery delays or complications.
Encore MedicalFeb 4, 2019 - Use cautionMedical device
Encore Medical, Lp recalls Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:
Encore Medical recalls specific revision hip implants due to loose proximal body bolts that may cause pain or need for additional surgery. Affected models include 495-00-065 to 495-01-085.
Encore MedicalSep 21, 2018 - Use cautionMedical device
Encore Medical, Lp recalls Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.
Encore Medical recalls flexible drill shafts with lot #262667L01 due to manufacturing error that may cause drill bits to come loose during surgery, risking delays or revision surgery.
Encore MedicalSep 19, 2018 - UnratedMedical device
Encore Medical, LP recalls djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgical Linear Neck
Encore Medical recalls djosurgical Linear Neck Trials with Spring Sides due to potential retaining ring failure. Affected models include REF S-200635 and S-200636. No remedy specified in recall notice.
djosurgicalJul 10, 2018 - Lower riskMedical device
Encore Medical, Lp recalls Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid
Encore Medical recalls instrument trays used in orthopedic surgery due to potential non-biocompatible black coating after cleaning. Affected units may pose health risks if used improperly.
Encore MedicalJun 26, 2018 - UnratedMedical device
Encore Medical, Lp recalls Foundation Modular Femoral Stem, Part Number, 220-10-110. Knee prosthesis component. The Foundation Revision Knee is a
Encore Medical recalls Foundation Revision Knee prosthesis component (part 220-10-110) due to lack of FDA clearance. This unapproved device may pose risks for patients needing knee replacements.
Encore MedicalMay 14, 2018 - Use cautionMedical device
Encore Medical, Lp recalls AltiVate Reverse INSTRUMENTATION, HUMERAL SOCKET SHELL TRIAL, STANDARD, REF 804-06-152, Qty: 01, Encore Medical, LP
Encore Medical recalls AltiVate Humeral Socket Shell Trial (REF 803-06-152) due to broken screws and retaining clips that may cause injury during surgery.
Encore MedicalJan 30, 2018 - UnratedMedical device
Encore Medical, Lp recalls Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Usage: The AltiVate
Encore Medical recalls Altivate Anatomic Shoulder Implants (size 50mm) due to a design flaw where pegs may not align properly with implants during surgery, potentially causing complications. Affected units include specific part numbers.
Encore MedicalJan 29, 2018 - Lower riskMedical device
Encore Medical, Lp recalls EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.
Encore Medical recalls EMPOWR Porous Knee System TIBIAL PUNCH, SMALL model for potential implant placement error during orthopedic surgery. Affected units may cause improper positioning of knee implants.
Encore MedicalDec 12, 2017 - Lower riskMedical device
Encore Medical, Lp recalls EMPOWR PS KNEE(TM) e+, REF 343-19-707, SIZE 7, 19mm, QTY 01, GREY, STERILE Product Usage The EMPOWR PS Inserts are
Encore Medical recalls EMPOWR PS Knee e+ inserts (REF 343-19-707) due to incorrect packaging with a different implant model. Affected units may have safety risks from mismatched components.
Encore MedicalSep 15, 2017 - Lower riskMedical device
Encore Medical, Lp recalls MODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers: REF S-200956 - 5mm PIN, SIZE 46 REF
Encore Medical recalls specific Turon Glenoid Reamer models with incorrect spherical radius cutting surface that may cause improper bone cutting during surgery.
Encore MedicalAug 4, 2017 - Lower riskMedical device
Encore Medical, Lp recalls Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS
Encore Medical recalls Cobalt HV with Gentamicin bone cement (REF 402283) due to potential packaging seal loss. This could compromise sterility during medical procedures. Affected patients should contact their doctor for guidance.
Encore MedicalJun 26, 2017 - Lower riskMedical device
Encore Medical, Lp recalls 3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are
Encore Medical recalls 3DKNEE System e+ Left Size 6 Tibial Insert (REF 391-11-706) due to mispacking: a Size 6 box contains a Size 8 insert. This affects patients using knee implants.
Encore MedicalMay 31, 2017
Encore Medical, LP recall questions
How many recalls has Encore Medical, LP had?
80 recalls from Encore Medical, LP are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Encore Medical, LP recall?
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product, dated Feb 16, 2026. Every Encore Medical, LP recall is listed on this page, newest first.
Why are Encore Medical, LP products recalled?
The most common reasons on record: Knee and Humeral socket implants contain incorrect labeling. (3); Due to packaging discrepancy with incorrect product size mixed up. (2); Knee implants contain incorrect labeling (size and/or side incorrect) (2); Mislabeling (2).
What should I do if I have a recalled Encore Medical, LP product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Encore Medical, LP recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.