Smiths Medical recalls TranStar SINGLE 84IN SET with anti-shunt stopcock due to potential inaccurate pressure monitoring. Affected units have specific product codes and lot numbers. Consumers should contact Smiths Medical for details.
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 SINGLE 84IN SET with anti-shunt stopcock because a manufacturing defect may cause inaccurate pressure readings or interruptions in monitoring. This could lead to incorrect medical decisions if used in critical care settings.
The device may have a leak or defect in the pressure transducer chip, causing inaccurate pressure readings. This could lead to incorrect medical decisions if used in critical care settings where precise pressure monitoring is essential.
Healthcare professionals using the TranStar set for blood pressure monitoring in critical care settings are most at risk. Patients receiving treatment with this device could be affected if the pressure readings are inaccurate.
Check the product code REF MXG300243R1 and lot numbers 4282765, 4307302, 4309198, 4311461, 4316668, 4328487, 4350011, 4366881 on the packaging or label.
Reach out to Smiths Medical for specific instructions on how to get a replacement or repair for the affected product.
The product code is REF MXG300243R1.
Affected lot numbers are 4282765, 4307302, 4309198, 4311461, 4316668, 4328487, 4350011, 4366881.
Due to a manufacturing defect that may cause inaccurate pressure monitoring or interruptions in pressure readings.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0203-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0203-2025 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.
