SEASPINE ORTHOPEDICS CORPORATION - SeaSpine Mariner RDX System - Class 2 Recall
Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX Deformity Head, REF: MX1-000040; Mariner RDX Extended Deformity Head, REF: MX1-000050; Mariner RDX Trauma Head, REF: MX1-000060; Mariner RDX Extended Trauma Head. REF: MX1-000070, part of Mariner RDX Alpha Instruments and Implants, REF: AMRDX and Mariner RDX TD Alpha Implants, REF: AMRDXTD, which are pedicle screw systems. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 23, 2024 Category: Medical Devices Source Type: alerts
DePuy Orthopaedics, Inc. - ATTUNE KNEE SYSTEM TIBIAL BASE AFFIXIUM FIXED BEARING SIZE 6 - Class 2 Recall
ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 30, 2024 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - Drill Bit - Class 2 Recall
1.5MM Drill Bit/QC/85MM Sterile-surgical, orthopedic, pneumatic powered & accessory/attachment Part Number: 310.15S (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 2, 2024 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - Drill Bit - Class 2 Recall
2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical, orthopedic, pneumatic powered & accessory/attachment Product Code: 310.25S (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 2, 2024 Category: Medical Devices Source Type: alerts
United Orthopedic Corporation - USTAR II Knee System PressFit Curved Stem, RHS Ti Plasma Spray - Class 2 Recall
USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9x150mm, PE25153113 - 13x125mm, PE25153111- 11x125mm, PE25153115 - 15x125mm, PE25153211 - 11x150mm, PE25153213 - 13x150mm, PE25153217 - 17x150mm, PE25153117 - 17x125mm, PE25153015 - 15x100mm, PE25153215 - 15x150mm (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 1, 2024 Category: Medical Devices Source Type: alerts
United Orthopedic Corporation - USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray - Class 2 Recall
USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211 - 11X150, PE25151213 - 13X150mm, PE25151215 - 15X150mm, PE25151217 - 17X150mm, PE25151415 - 15x200mm (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 1, 2024 Category: Medical Devices Source Type: alerts
United Orthopedic Corporation - USTAR II Hip System PressFit Curved Stem, RHS Ti Plasma Spray - Class 2 Recall
USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213 - 13x150mm, PE11151215 - 15x150mm, PE11151217 - 17x150mm, PE11151411 - 11x200mm, PE11151413 - 13x200mm, PE11151415 - 15x200mm, PE11151417 - 17x200mm, (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 1, 2024 Category: Medical Devices Source Type: alerts
HAV EZ PENETRATING PAIN RELIEF (menthol) gel [PALM ORTHOPEDICS & INTERVENTIONAL PAIN LLC]
Updated Date: Fri, 02 Feb 2024 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 2, 2024 Category: Drugs & Pharmacology Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178406 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Short Anchor Plug, 16 MM- Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement Item Number: 178558 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178565 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178410 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178566 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Short Anchor Plug, 12 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178554 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
Biomet, Inc. - OSSTM Compress & Mini Compress Anchor Plugs - Class 2 Recall
Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178568 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 22, 2023 Category: Medical Devices Source Type: alerts
