[Recalled] medex TranStar Stopcock w/Ext. 10/EA, Product Code REF MXG300242 — Due to a manufacturing defect, users may experience inaccurate pressure monitor… | FDA 2024-09-24
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | medex TranStar Stopcock w/Ext. 10/EA, Product Code REF MXG300242 |
|---|---|
| Brand / manufacturer | Smiths Medical ASD, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0202-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 September 2024 |
| EAN / barcode | 50351688517782 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Smiths Medical ASD, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.