Class II

Medical Device Recall: medex TranStar MONITORING SET W/SAMPLING PORT 10/EA, Product Code REF MXG300260

Smiths Medical ASD, Inc. · September 24, 2024

Reason for Recall

Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within the TranStar Disposable Pressure Transducer or from a defect within the TranStar Disposable Pressure Transducer chip.

Distribution

Worldwide distribution.

Quantity Affected

1640 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0204-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.