Smiths Medical recalls TranStar 72in Double Monitoring Kit 10/EA due to potential inaccurate pressure readings from a manufacturing defect in the pressure transducer.
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.
Smiths Medical is recalling TranStar 72in Double Monitoring Kits because a manufacturing defect may cause inaccurate pressure readings or interruptions in monitoring. This could lead to incorrect medical decisions if the device is used for critical patient monitoring.
The device may show incorrect pressure readings due to a leak or defect in the pressure transducer chip. This could lead to improper medical decisions if the device is used for critical patient monitoring.
Healthcare professionals using the TranStar 72in Double Monitoring Kit for patient monitoring are most at risk. Patients receiving critical care with this device could be affected if the monitoring is inaccurate.
Check for the product code REF MX9502T on the kit. The lot numbers 4270150, 4277661, 4277716, and 4287633 are associated with this recall.
Verify the product code REF MX9502T and lot numbers 4270150, 4277661, 4277716, or 4287633 to confirm if your kit is affected.
Smiths Medical recalls the TranStar 72in Double Monitoring Kit due to a manufacturing defect that may cause inaccurate pressure readings or interruptions in monitoring.
Check the product code and lot numbers to see if your kit is affected. If it is, contact Smiths Medical for further instructions.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0190-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0190-2025 from Smiths Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
