Orthosensor Recalls
8 recalls on record · October 31, 2012 to October 17, 2018 · Medical Devices
Recalls by year
12
15
18
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right, REF ZBH-PSNCRGH712-R.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left, REF ZBH-PSNCRGH712-L.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, REF ZBH-PSNCRCD39-R.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, REF ZBH-PSNCRCD39-L.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, REF ZBH-PSNCREF311-R.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
October 17, 2018Medical DevicesFDA
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
Hazard: Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
February 4, 2015Medical DevicesFDA
Orthosensor, Inc. recalls Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during ortho
Hazard: Presence of one inoperable (dead) sensor pad.
October 31, 2012Medical DevicesFDA
Orthosensor recalls "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL 33323***w
Hazard: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface Software 1.8 (which was updated to version 1.82, validated on 02/13/12). Recall was initiated due to customer feedback which included the line of site between the knee ba lancer and the Link station was obstructed by OR metal stands or trays or the knee balancer device was placed atop of or near the metal stands or trays, interru