[Recalled] L12-5 38mm Transducer Probe — To provide clarification and labelling to define the useful life of ultrasound… | FDA 2025-07-03
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | L12-5 38mm Transducer Probe |
|---|---|
| Brand / manufacturer | Philips Ultrasound, Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2375-2025 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 03 July 2025 |
| EAN / barcode | 989605428532 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
This Class III 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 Philips Ultrasound, 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.