Steris Corporation - OT Surgical Table - Class 2 Recall
OT1000 Series Orthopedic Surgical Tables (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 25, 2021 Category: Medical Devices Source Type: alerts
DePuy Orthopaedics, Inc. - Universal Femoral Sleeve Full Porous - Class 2 Recall
Universal Femoral Sleeves - Product Usage: used primarily in revision surgeries with the S-ROM Noiles, LPS, SIGMA, and LCS Knee products. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 10, 2021 Category: Medical Devices Source Type: alerts
Biomet, Inc. - A.L.P.S. Clavicle Plating System - Class 2 Recall
A.L.P.S. Clavicle Plating System, Plate, Fixation, Bone, Item Number 233500004 - Product Usage: indicated for fixation of fractures, osteotomies and non-unions of the clavicle including osteopenic bone. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 22, 2021 Category: Medical Devices Source Type: alerts
DePuy Orthopaedics, Inc. - Pinnacle Hip System - Class 2 Recall
Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048 121711052 121712050 121712052 121712056 121722048 121722050 121722052 121722054 121722056 121722058 121722060 121722062 121731048 121731050 121731052 121731054 121731056 121731058 121731060 121731062 121732048 121732050 121732052 121732054 121732056 121732058 121732060 121732062 121732064 - Product Usage: The PINNACLE CUP devices are part of the Pinnacle Hip Solution for the anatomic reconstruction of the hip joint, which promotes prosthetic joint load and function. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 8, 2021 Category: Medical Devices Source Type: alerts
Smith & Nephew, Inc. - TRIGEN INTERTAN - Class 2 Recall
Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fracture; (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 7, 2021 Category: Medical Devices Source Type: alerts
Zimmer Biomet, Inc. - Spinal Rod Cutter - Class 2 Recall
Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of this instrument is to be used for cutting orthopedic rods/pins during orthopedic surgeries. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 23, 2020 Category: Medical Devices Source Type: alerts
Biomet, Inc. - PHOENIX - Class 2 Recall
PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long bones. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 18, 2020 Category: Medical Devices Source Type: alerts
Biomet, Inc. - 3.0mm Cannulated Screw System - Class 2 Recall
3.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009787 110009790, 110009794, 110009796, 110009798, 110009800 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 18, 2020 Category: Medical Devices Source Type: alerts
Biomet, Inc. - 6.5/8.0mm Cannulated Screw System - Class 2 Recall
6.5/8.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009929, 110009934, 110009935, 110009936, 110009993, 110009994, 110009996, 110009998, 110010000, 110010003, 110010029, 110010030, 110010032, 110010099 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 18, 2020 Category: Medical Devices Source Type: alerts
Biomet, Inc. - Comprehensive Reverse Shoulder System - Class 2 Recall
Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, 180552, 180553, 180554, 180555, 180556, 180557, 180558, 180559, 180560, 180562 - Product Usage: indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthroplasty and/or previously failed shoulder joint replacement with a grossly deficient rotator cuff The patient must anatomically and structurally suited to receive the implants and a functional deltoid muscle is necessary. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 18, 2020 Category: Medical Devices Source Type: alerts
Biomet, Inc. - 4.0/5.0mm Cannulated Screw System - Class 2 Recall
4.0/5.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009810, 110009821, 110009825, 110009852 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 18, 2020 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - DePuy Synthes - Class 2 Recall
DePuy Synthes 13.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.022S (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 16, 2020 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - DePuy Synthes - Class 2 Recall
DePuy Synthes 16.0MM REAMER HEAD FOR RIA 2 STERILE--Orthopedic manual surgical instrument Part Code: 03.404.028S (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 16, 2020 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - DePuy Synthes - Class 2 Recall
DePuy Synthes 13.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.023S (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 16, 2020 Category: Medical Devices Source Type: alerts
Synthes (USA) Products LLC - DePuy Synthes - Class 2 Recall
DePuy Synthes 10.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.017S (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 16, 2020 Category: Medical Devices Source Type: alerts
