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Recall Observatory FDA recall evidence

Device product

medex Arterial Kit 1/EA, Product Code REF MX7827

Z-0187-2025

September 24, 2024

Class II

Product summary

Firm
Smiths Medical ASD, Inc.
Event
Event 95438
Status
Ongoing
Classification
Class II
Quantity
2232 units
Official record key
device-enforcement:Z-0187-2025

Official wording

Reason: 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.

Code information: UDI/DI 50351688505185 (case), 10351688505187 (pouch), Lot Numbers: 4282733, 4319605, 4340472, 4355338, 4390060, 4411161

Distribution pattern: Worldwide distribution.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect