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INTERLINK SYSTEM T-CONNECTOR EXTENSION SET Adverse Event — Malfunction (MDR 1416980-2020-02427)

INTERLINK SYSTEM T-CONNECTOR EXTENSION SET Adverse Event — Malfunction (MDR 1416980-2020-02427) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTERLINK SYSTEM T-CONNECTOR EXTENSION SET; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BAXTER HEALTHCARE CORPORATI

DeviceINTERLINK SYSTEM T-CONNECTOR EXTENSION SET
Generic nameSET, ADMINISTRATION, INTRAVASCULAR
ManufacturerBAXTER HEALTHCARE CORPORATION
Report number1416980-2020-02427
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeADDITIONAL INFORMATION: H6 THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
SourceopenFDA MAUDE (device adverse events)

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