[Recalled] Ingenuity TF PET/CT Model # 882456, computed tomography x-ray system — In certain instances when performing a cardiac step and shoot acquisition with… | FDA 2019-06-24
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Ingenuity TF PET/CT Model # 882456, computed tomography x-ray system |
|---|---|
| Brand / manufacturer | Philips Medical Systems (Cleveland) Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2193-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 June 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: In certain instances when performing a cardiac step and shoot acquisition with phase tolerance selected, images may be labeled as if phase tolerance had been applied when phase tolerance had not been applied
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 Philips Medical Systems (Cleveland) 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.