FDA Device recall Z-0185-2025
medex TRANSTAR MONITORING KIT 1/EA, Product Code REF MX20103R1
- FDA Device
- Class II
- ongoing
- Published 2024-10-30
On 2024-10-30 the FDA classified a Class II recall of medex TRANSTAR MONITORING KIT 1/EA, Product Code REF MX20103R1 by Smiths Medical Asd, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0185-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-09-24 |
| Published | 2024-10-30 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Smiths Medical Asd |
| Distribution | n/a |
Product
medex TRANSTAR MONITORING KIT 1/EA, Product Code REF MX20103R1
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.
Identifiers
| code_info | UDI/DI 50351688551694 (case), 10351688551696 (pouch), Lot Numbers: 4270117 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0185-2025%22
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