Aesculap Implant Systems recalls
Aesculap Implant Systems appears in 62 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- ELAN 4 Blade: ELAN 4 1-RING PIN CUTTER D1.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D1.5 ELAN 4 1-RING NEURO CUTTER+ SOFT D2.0 ELAN 4 1-RING NEURO…
FDA Device · Class II · 2018-02-21 · Aesculap Implant Systems - GP321R
FDA Device · Class II · 2017-05-24 · Aesculap Implant Systems - GP161R
FDA Device · Class II · 2017-05-24 · Aesculap Implant Systems - GE426R
FDA Device · Class II · 2017-05-24 · Aesculap Implant Systems - AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures…
FDA Device · Class II · 2017-04-19 · Aesculap Implant Systems - GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
FDA Device · Class II · 2017-02-22 · Aesculap Implant Systems - Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is inten…
FDA Device · Class II · 2017-01-11 · Aesculap Implant Systems - Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture
FDA Device · Class II · 2016-11-02 · Aesculap Implant Systems - Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T, ST241T, ST242T, ST243T, ST244T, and ST245T). The S4 Spinal System is intended for anter…
FDA Device · Class II · 2012-09-19 · Aesculap Implant Systems - Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant (SJ780T-US) Product Usage: The Aesculap Implant S…
FDA Device · Class II · 2012-08-08 · Aesculap Implant Systems - S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Revision Instruments assist in the removal of an occipital cervical scr…
FDA Device · Class II · 2012-07-11 · Aesculap Implant Systems - Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Columbus Revision Knee System is indicated for…
FDA Device · Class II · 2012-06-20 · Aesculap Implant Systems