Synthes USA HQ, Inc. - Class 2 Recall
Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the Multi Vector Distractor which cis used for mandibular bone lengthening, including conditions such as congenital mandibular deficiencies or post-traumatic defects. The Multi Vector Distractor can be utilized to perform bone transport procedures as an alternative to bone grafts and free flaps. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 18, 2013 Category: Medical Equipment Source Type: alerts
SpineFrontier, Inc. - SLIFT - Class 2 Recall
S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instrument to add further compression of the Inserter into the Implant during implantation of S-LIF Intervertebral Body Fusion Devices using bone graft to facilitate fusion of the spine of skeletally mature patients. Model: SI50003 RevA (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 6, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, LARGE II KIT, REF 7510800AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, SMALL KIT, REF 7510200AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Medtronic Sofamor Danek USA Inc - INFUSE(R) Bone Graft - Class 2 Recall
INFUSE(R) Bone Graft,LARGE II KIT, REF 7510800, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 26, 2013 Category: Medical Equipment Source Type: alerts
Alphatec Spine, Inc. - IILICO MIS Posterior Spinal Fixation System - Class 2 Recall
ILLICO Straight CP TI Rod, -5.5MM x 110M; REF#73601-110; Qty 1; LBL-005; REV.B; RX ONLY; Alphatec Spine, Inc. The ILLICO¿ MIS Posterior Spinal Fixation System is intended to facilitate the surgical correction of non-cervical spinal deformities by providing temporary internal fixation and stabilization during bone graft healing and/or fusion mass development. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 19, 2013 Category: Medical Equipment Source Type: alerts
Biomet, Inc. - Arthrotek Interference Screw - Class 2 Recall
TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal fixation devices intended to aid in arthroscopic and orthopedic reconstructive procedures requiring soft tissue fixation, due to injury or degenerative disease. Implants used for this application include: screws, washers, anchors, pins, and suture. Interference Screws and Set Screws are intended for use in fixation of patellar bone-tendon-bone grafts in ACL reconstruction. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 31, 2013 Category: Medical Equipment Source Type: alerts
Surgical Tissue Network, Inc. - UltraFill DBM - Class 2 Recall
UltraFill DBM labeled in part: "***TISSUENET***Sterilized by T10^6 (r)***Description: UltraFill DBM***Size: 10cc***Product Code: RT53010***Donated Human Tissue Allograft***SINGLE PATIENT USE ONLY***FOR INTERNATIONAL USE ONLY***See Package Insert for Additional Information***" TissueNet's Porcine DBM product line is used as a bone void filler. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 8, 2013 Category: Medical Equipment Source Type: alerts
Surgical Tissue Network, Inc. - Ultrafill DBM - Class 2 Recall
Ultrafill DBM labeled in part: "***TISSUENET***Sterilized by T10^6 (r)***Description: UltraFill DBM***Size: 1cc***Product Code: RT53001***Donated Human Tissue Allograft***SINGLE PATIENT USE ONLY***FOR INTERNATIONAL USE ONLY***See Package Insert for Additional Information***" TissueNet's Porcine DBM product line is used as a bone void filler (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 8, 2013 Category: Medical Equipment Source Type: alerts
Surgical Tissue Network, Inc. - UltraFill DBM - Class 2 Recall
UltraFill DBM labeled in part: "***TISSUENET***Sterilized by T10^6 (r)***Description: UltraFill DBM***Size: 5cc***Product Code: RT53005***Donated Human Tissue Allograft***SINGLE PATIENT USE ONLY***FOR INTERNATIONAL USE ONLY***See Package Insert for Additional Information***" TissueNet's Porcine DBM product line is used as a bone void filler. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 8, 2013 Category: Medical Equipment Source Type: alerts
