Class II

Medical Device Recall: medex TranStar Patient Mount Monitoring Kit 10/EA, Product Code REF MX9501T

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

1740 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0189-2025

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.

Smiths Medical ASD, Inc. Medical Device Recall: medex TranStar Patient Mount Monitoring Kit 10/EA, Product Code REF MX9501T | SafeCheck