사례

이름 날짜 시작된 날짜 국가 출처
Device Recall SpineFrontier PedFuse Pedicle Screw System 의 리콜 2014-12-19 United States USFDA
Device Recall AntiLambda APCH7 의 리콜 2014-12-19 United States USFDA
Device Recall BD CD8 (SK1) phycoerythrin (PE) 의 리콜 2014-12-19 United States USFDA
Device Recall MAQUET Servo Humidifier 163 의 리콜 2014-12-04 United States USFDA
Device Recall Baxter 의 리콜 2014-12-29 United States USFDA
Device Recall Hemostatic Bone Putty 의 리콜 2012-01-06 United States USFDA
Device Recall SpermMar Test 의 리콜 2014-12-22 United States USFDA
Device Recall GE Revolution CT computed tomography xray systems 의 리콜 2014-11-12 United States USFDA
Device Recall Fitness Gear Inversion table 의 리콜 2014-12-29 United States USFDA
Device Recall LINAC Accelerators 의 리콜 2014-12-19 United States USFDA
Device Recall Clinical Innovations 의 리콜 2014-12-30 United States USFDA
Device Recall Zippie Zone Pediatric Rigid Wheelchair 의 리콜 2014-12-19 United States USFDA
Device Recall Quickie Q7 Adult Rigid Wheelchair 의 리콜 2014-12-19 United States USFDA
Device Recall McKesson Cardiology ECG Management 의 리콜 2014-12-19 United States USFDA
Device Recall Shape Disposable Patient Interface 의 리콜 2014-12-23 United States USFDA
Device Recall Penner 의 리콜 2015-01-30 United States USFDA
Device Recall Protektor 32 (EPWorks software) 의 리콜 2015-01-02 United States USFDA
Device Recall Xltek Protektor Stimulator (EPWorks software) 의 리콜 2015-01-02 United States USFDA
Device Recall Portable Oxygen System regulators: OxyTOTE, OxyTOTE 3000, OxyTOTE NG, OxyTOTE 3000 NG 의 리콜 2015-01-31 United States USFDA
Device Recall BD Viper LT System 의 리콜 2014-11-07 United States USFDA
Device Recall MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm 의 리콜 2014-12-17 United States USFDA
Device Recall MEDPOR BARRIER Sheets Orbital Floor Implant 의 리콜 2014-12-17 United States USFDA
Device Recall MEDPOR BARRIER Sheets Rectangle 의 리콜 2014-12-17 United States USFDA
Device Recall MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPORTitaniumBarrier (MTB) Right 의 리콜 2014-12-17 United States USFDA
Device Recall ARROWgard Blue PLUS Pressure Injectable TwoLumen CVC Kit 의 리콜 2015-01-02 United States USFDA