Smiths Medical recalls TranStar 84in Single Monitoring Kit (Product Code REF MX9505T) due to potential inaccurate pressure monitoring from manufacturing defects 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 84in Single Monitoring Kits because a manufacturing defect may cause inaccurate pressure readings, interruptions in monitoring, or inability to zero the device. 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 leaks or defects in the disposable pressure transducer or its internal chip. This could cause healthcare providers to make wrong medical decisions, such as underestimating or overestimating a patient's blood pressure.
Healthcare providers using the TranStar 84in Single Monitoring Kit for patient monitoring are most at risk, particularly those in settings where accurate blood pressure readings are critical.
Check for the product code REF MX9505T on the kit. The lot numbers listed in the recall include specific sequences like 4277670 through 4355757. The kit comes in a case with UDI/DI 50351688503990 and a pouch with 10351688503992.
Verify the product code REF MX9505T and lot numbers listed in the recall to confirm if your kit is affected.
Reach out to Smiths Medical directly for further assistance or to confirm if your specific kit needs replacement.
The recall is due to a manufacturing defect that may cause inaccurate pressure monitoring, interruptions in pressure readings, or an inability to zero the device.
Check the product code and lot numbers listed in the recall to see if your kit is affected. Contact Smiths Medical for further instructions.
The recall does not specify a fix; the remedy is null, so users should contact the manufacturer for guidance.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0192-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0192-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
