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Unetixs Vascular, Inc. recalls MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01
Recalled March 8, 2023 · FDA recall Z-1194-2023 · Unetixs Vascular
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. · FDA Class II
Units
2310 units
Sold at
Worldwide distribution - US Nationwide and Global distribution.
Description
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.
Product
MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01
Manufacturer(s)
Unetixs Vascular, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →