Smiths Medical recalls TranStar DPT pressure monitors with potential inaccurate readings due to manufacturing defects. 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 DPT pressure monitors that may give inaccurate pressure readings. This defect could lead to incorrect medical monitoring, which is serious for patients using the device.
The device may have leaks or defects in its pressure transducer chip, causing inaccurate pressure readings. This could lead to incorrect medical monitoring, which is serious for patients relying on the device.
Patients using the TranStar DPT pressure monitor for medical monitoring are most at risk. The recall affects specific product codes and lot numbers sold through medical suppliers.
Check for product code REF MX950SCNT and lot numbers 4293126, 4309186, 4316649, 4323123, 4328467, or 4346049. The device comes in a case with UDI/DI 50351688503938 and a pouch with 10351688503930.
Look for product code REF MX950SCNT and lot numbers listed in the recall notice.
Due to a manufacturing defect, the TranStar DPT may have leaks or defects in its pressure transducer chip, causing inaccurate pressure readings.
Contact Smiths Medical directly for details on the specific product code and lot numbers to confirm if it's affected.
The recall record does not specify a remedy, so no fix is provided. Affected users should contact Smiths Medical for further instructions.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0194-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0194-2025 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.
