223 results
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17ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration start-up issue; Azurion R2.2 emergency stop recovery issue Model Numbers: 722221, 722228, 722225, 722068, 722226, 722078, 722224
FDA Recall
Terminated
·Philips North America Llc·Product code OWB·November 12, 2021
Cable remote control JUC, BUTTON, Material no.1239823, Serial number: to (incl.) 100143048. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
FDA Recall
Terminated
·Trumpf Medical Systems, Inc.·Product code JEA·December 3, 2014
IR remote control JUC, BUTTON, Material no.1239824, Serial number: to (incl.) 100139854. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
FDA Recall
Terminated
·Trumpf Medical Systems, Inc.·Product code JEA·December 3, 2014
Vital Signs- A GE Healthcare Company - Hygroscopic Condenser Humidifier (HCH)/Anesthesia Breathing Circuit; GE Medical Systems SCS 283 rue de la Miniere 78530 BUC, France p +33.1.30.70.40.40; Vital Signs Colorado Inc 11039 E. Lansing Circle Englewood, CO 80112 P +1.973.956.5300. The intended use of the device is to provide proper flow of the medical gases or oxygen to patients under anesthesia or ventilation.
FDA Recall
Terminated
·Vital Signs Devices, a GE Healthcare Company·Product code BYD·April 29, 2011
United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025
FDA Recall
Terminated
·Uoc Usa Inc·Product code KRO·August 27, 2021
Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·March 13, 2024
8MM,CADIERE FORCEPS,IS4000 REF 470049
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,TENACULUM FORCEPS,IS4000 REF 470207
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,PROGRASP FORCEPS,IS4000 REF 471093
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,SMALL GRASPING RETRACTOR,IS4000 REF 470318
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,FENESTRATED BIPOLAR FORCEPS,IS4000 REF 471205
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,DEBAKEY FORCEPS,IS4000 REF 470036
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,MARYLAND BIPOLAR FORCEPS,IS4000 REF 471172
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,CADIERE FORCEPS,IS4000 REF 471049
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,PROGRASP FORCEPS,IS4000 REF 470093
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,LONG BIPOLAR GRASPER,IS4000 REF 471400
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,MEDIUM-LARGE CLIP APPLIER,IS4000 REF 470327
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,FENESTRATED BIPOLAR FORCEPS,IS4000 REF 470205
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,HORIZON SMALL CLIP APPLIER,IS4000 REF 470401
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024
8MM,MICRO BIPOLAR FORCEPS,IS4000 REF 470171
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code NAY·December 19, 2024