Every recall we track for Encore Medical, LP — 80 in all — plus the complaints and injury reports the public filed about them.
Encore Medical recalls EMPOWR 3D Knee Ins 11L 14MM VE model 341-14-711 due to incorrect product size packaging. Affected units include specific lot codes with expiration dates through June 2026.
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 Medical recalls EMPOWR 3D KNEE knee implants with incorrect labeling. Affected models include 341-16-707 (Lot 151T1055A). Correct labeling is critical for safe use.
Encore Medical recalls RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus due to incorrect labeling on knee and humeral socket implants. Affected units have model 509-00-036 and lot 378P1382.
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 Medical recalls certain EMPOWR Acetabular System liners due to packaging discrepancies that could lead to surgical delays or revision surgery. Affected units include specific model numbers and reference codes.
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.
DJO SURGICAL recalls ALTIVATE REVERSE WEDGE GLENO: 804-06-310 due to potential binding during use. This may cause injury. Consumers should contact DJO SURGICAL for details.
DJO SURGICAL recalls ALTIVATE REVERSE WEDGE GLENO: Model 804-06-311. Potential for reamer to kick or bind during use, causing injury. Consumers should contact DJO SURGICAL for details.
DJO SURGICAL recalls FA S Altivate Reverse Glenoid Tray due to potential reamer binding during or before surgery, which could cause injury. Affected patients should contact the manufacturer for details.
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.
Encore Medical recalls EMPOWR 3D Knee TIBIAL INSERT E-PLUS model 342-16-707 with incorrect size or side labeling. This may lead to improper implant use during knee replacement surgery.
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 Medical recalls EMPOWR Dual Mobility hip implants with incorrect tibial inserts due to packaging error. Affected units may have safety risks from improper implant fit.
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.
Encore Medical recalls EMPOWR 3D KNEE TIBIAL INSERT E-PLUS model 341-10-711 due to packaging error that may cause incorrect product selection and revision surgery.
Encore Medical recalls EMPOWR 3D knee tibial inserts due to packaging errors that may lead to incorrect product selection and revision surgery.
Encore Medical recalls ALTIVATE REVERSE Torx Peripheral screws (model 506-04-122) due to incorrect size labeling on packaging. This may lead to improper use in shoulder replacements.
Encore Medical recalls ALTIVATE REVERSE Torx Peripheral screws (model 506-04-118) due to incorrect size labeling on packaging. This may lead to improper use in shoulder replacements.
Encore Medical recalls ALTIVATE REVERSE Torx Peripheral Screws (model 506-04-130) due to incorrect labeling. This may cause confusion in medical use. Contact for details.
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 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 Medical recalls EMPOWR 3D Knee Tibial Insert 6R 10MM model due to potential surgical delay from an acetabular system in the package.
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.
Encore Medical recalls sterile H2O2 products due to mislabeling. Affected items have specific UDI and lot numbers. Consumers should check their product details.
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 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 Medical recalls specific orthopedic shoulder implant components due to potential mix-up in packaging that could delay surgery. Affected items have unique identifiers; contact for details.
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.
DJO Surgical recalls RSP Glenoid Baseplate model 508-32-204 due to coating hex not engaging with standard tools, risking improper installation.
Encore Medical recalls EMPOWR 3D Knee Tibial Insert (REF: 342-10-705) due to swapped hip/knee parts risking wrong surgery product. Affected units have specific UDI-DI and lot numbers.
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 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.
DJO Surgical recalls Altivate Reverse Humeral Stem (Size 6 x 108mm) due to potential infection from improper sterilization. Affected units have UDI-DI/Lot: 00190446259091/923W1411 from April 2029. Contact for replacement.
DJO Surgical recalls reverse shoulder system components due to potential infection from unsterilized parts. Affected items include specific semi-humeral socket inserts and baseplates with serial numbers ending in 00888912024693, 00888912024754, and 00888912024754.
DJO Surgical recalls hip implants (Size#3) with potential infection risk. Affected units have specific UDI-DI/Lot/Expiration codes. Contact for details on safety.
DJO Surgical recalls Delta Ceramic Femoral Head implants (44mm + 4.0mm) due to potential infection from improper sterilization. Affected units have specific UDI-DI/Lot/Expiration codes. Contact for return or repair.
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.
Encore Medical recalls two EMPOWR knee drills due to incorrect diameter markings that could cause implant loosening or bone fractures during surgery.
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 Medical recalls EMPOWER 3D Knee Tibial Insert REF 341-14-708 due to potential surgery delays from incorrect implant mix-ups.
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 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 Medical recalls AltiVate Anatomic Shoulder System parts due to humeral stem failing to mate with broach handles, potentially causing procedure delays or revision surgery.
DJO Surgical recalls EMPOWR 3D Knee Tibial Insert e-plus (REF 341-16-711) due to packaging mixup where 12mm and 16mm knee prostheses may be swapped. Affected units include specific sizes and lot numbers.
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.
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 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 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 Medical recalls RSP Standard Humeral Socket Insert (40mm) due to potential size mismatch with patient labels, risking incorrect implantation and surgery complications.
Encore Medical recalls RSP Standard Humerus Socket Insert (44mm) due to possible size mismatch with patient labels, risking incorrect implant and surgery complications.
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.
Encore Medical recalls EMPOWR Partial Knee Peg Drill model 800-06-008 due to potential drilling issues that could delay surgery. All units are affected.
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 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 Medical recalls EMPOWR Locking Femoral Impactor parts due to breakage risks and potential misalignment causing surgery delays or complications.
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 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 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.
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.
