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Unetixs Vascular Recalls
4 recalls on record · March 8, 2023 to March 8, 2023 · Medical Devices
March 8, 2023Medical DevicesFDA
Unetixs Vascular, Inc. recalls MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01
Hazard: The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
March 8, 2023Medical DevicesFDA
Unetixs Vascular, Inc. recalls MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01
Hazard: The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
March 8, 2023Medical DevicesFDA
Unetixs Vascular, Inc. recalls MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01
Hazard: The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
March 8, 2023Medical DevicesFDA
Unetixs Vascular, Inc. recalls MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-0000-01
Hazard: The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.