Dispositivos

Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall 3.2MM X 510MM COCR THD TIP Orthopedic Devices Zimmer Biomet, Inc. 2 United States
Device Recall RECON DRILL 6MM X 439MM Orthopedic Devices Zimmer Biomet, Inc. 2 United States
Device Recall 3.2MM X 560MM COCR THD TIP Orthopedic Devices Zimmer Biomet, Inc. 2 United States
Device Recall Farabeuf Clamp for 3.5mm Screws PRO General and Plastic Surgery Devices Stryker GmbH 1 United States
Device Recall Cryovalve(R) SG Pulmonary Human Heart Valve Cardiovascular Devices CryoLife, Inc. Unclassified United States
Device Recall Cryopatch SG Pulmonary Human Cardiac Patch Cardiovascular Devices CryoLife, Inc. 2 United States
Device Recall RayStation Radiology Devices RAYSEARCH LABORATORIES AB 2 United States
Device Recall Biograph mCT Systems: Radiology Devices Siemens Medical Solutions USA, Inc. 2 United States
Device Recall STATCheck MANUAL RESUSCITATOR / VENTILATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall MEDLINE ADULT MANUAL RESUSCITATOR Anesthesiology Devices Sun Med, LLC 2 United States
Device Recall Spiralgold Jostra-Bentley Corporation United States
Lots 2223041 and 2244061 of the "Seraclone Anti-S" reagent, Reference No. 808052 Bio-RAd Medical Diagnostics GmbH Spain