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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall PKG, BIPOLAR FORCEPS, MICRO TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, STRAIGHT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OBTURATOR, 11MM, FOR HASSON CANNULA, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 5MM INSERT, BOWEL GRASPER FORCEPS, 45CM, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 3.5MM CANNULA AUTO VALVE, STOPCOCK, SHORT, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 3.5MM TROCAR, PYRAMIDAL TIP, SHORT, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 5MM INSERT, RETENTION GRASPER, 33CM Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 5MM X 45CM INSERT, ALLIS FORCEPS, DOUBLE ROW TEETH, Stryker Endoscopy 2 United States USFDA
Device Recall GE Inspection Technologies Phoenix vtomex M240 cabinet xray systems. GE Inspection Technologies, LP Not Classified United States USFDA
Bard Orbiter PV Steerable Catheter || Item #: 320100 (Marketed in Europe Only) C. R.Bard, Inc./Electrophysiology Division United States USFDA
Device Recall Boston Scientific /Micorvasive Boston Scientific Corporation United States USFDA
Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. || Kit: AMPLICOR M. avium Detection Kit, Export,RUO. Roche Molecular Systems Inc United States USFDA
VITEK 2 AST P612 Biomerieux Inc United States USFDA
VITEK 2 AST N190 Biomerieux Inc United States USFDA
VITEK 2 AST N230 Biomerieux Inc United States USFDA
VITEK 2 AST P625 Biomerieux Inc United States USFDA
VITEK 2 AST N330 Biomerieux Inc United States USFDA
Device Recall H. Pylori Ab Test CardSerum LumiQuick Diagnostics Inc. United States USFDA
Device Recall Methamphetamine Strip LumiQuick Diagnostics Inc. United States USFDA
Device Recall Propoxyphene Test Strip LumiQuick Diagnostics Inc. United States USFDA
Device Recall Troponin I test Card (Whole Blood) LumiQuick Diagnostics Inc. United States USFDA
Device Recall Matrix MAX 3 Skf USA Inc United States USFDA
Device Recall Matrix MAX 3 Skf USA Inc United States USFDA
Device Recall Epic II VR Model V158 St Jude Medical CRMD United States USFDA