Every recall we track for Unetixs Vascular, Inc. — 4 in all — plus the complaints and injury reports the public filed about them.
Unetixs Vascular recalls MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic devices due to potential air embolism risk from misconnected IV lines. Affected units have model number 11949-0000-01 and all serial numbers.
Unetixs Vascular recalls MultiLab Series II REVO non-invasive vascular diagnostic device (Model 12950-0000-01) due to risk of air embolism from misconnected IV lines.
Unetixs Vascular recalls MultiLab Series II 2CP and 2CP Express devices due to risk of air embolism if air line connects to IV lines. All units with model 11996-0000-01 are affected.
Unetixs Vascular recalls MultiLab Series II ROODRA non-invasive vascular diagnostic device (Model 11986-0000-01) due to risk of air embolism from misconnected IV lines. All units with serial numbers are affected.
