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LIBERTY CYCLER SET, DUAL PATIENT CONNECT Adverse Event — Malfunction (MDR 8030665-2020-00562)

LIBERTY CYCLER SET, DUAL PATIENT CONNECT Adverse Event — Malfunction (MDR 8030665-2020-00562) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LIBERTY CYCLER SET, DUAL PATIENT CONNECT; Generic name: SYSTEM, PERITONEAL, AUTOMATIC DELIVERY; Manufacturer: ERIKA DE REYNOSA, S.A. DE C

DeviceLIBERTY CYCLER SET, DUAL PATIENT CONNECT
Generic nameSYSTEM, PERITONEAL, AUTOMATIC DELIVERY
ManufacturerERIKA DE REYNOSA, S.A. DE C.V.
Report number8030665-2020-00562
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeTHE PLANT INVESTIGATION IS IN PROCESS. A SUPPLEMENTAL MDR WILL BE SUBMITTED UPON COMPLETION OF THIS ACTIVITY.
SourceopenFDA MAUDE (device adverse events)

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