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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall T/S2 0.9 Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL General Hospital and Personal Use Devices MRP, LLC dba AMUSA 2 United States USFDA
Device Recall 0.9 Sodium Chloride Injection, USP General Hospital and Personal Use Devices MRP, LLC dba AMUSA 2 United States USFDA
0.9 Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile General Hospital and Personal Use Devices MRP, LLC dba AMUSA 2 United States USFDA