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BD CONNECTA STOPCOCK Adverse Event — Malfunction (MDR 9610847-2020-00141)

BD CONNECTA STOPCOCK Adverse Event — Malfunction (MDR 9610847-2020-00141) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD CONNECTA STOPCOCK; Generic name: STOPCOCK; Manufacturer: BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V..

DeviceBD CONNECTA STOPCOCK
Generic nameSTOPCOCK
ManufacturerBD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.
Report number9610847-2020-00141
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceFOREIGN, OTHER, USER FACILITY
NarrativeA DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.
SourceopenFDA MAUDE (device adverse events)

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