Z-0195-2025 Class II Ongoing

Recalled by Smiths Medical ASD, Inc. — Minneapolis, MN

FDA device recall Z-0195-2025 was initiated by Smiths Medical ASD, Inc. on September 24, 2024 and is designated Class II. Reason for recall: 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 … The recall status is ongoing. Affected quantity: 1110 units.

Recall Details

Product Type
Devices
Report Date
October 30, 2024
Initiation Date
September 24, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1110 units

Product Description

medex TranStar DPT w/Two Stopcocks 10/EA, Product Code REF MX950X2SC

Reason for Recall

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.

Distribution Pattern

Worldwide distribution.

Code Information

UDI/DI 50351688503921 (case), 10351688503923 (pouch), Lot Numbers: 4363257, 4385760