[Recalled] Biograph 16 TruePoint - 3R, Material Number 10249555 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emi
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Biograph 16 TruePoint - 3R, Material Number 10249555 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the purpose of determining var |
|---|---|
| Brand / manufacturer | Siemens Medical Solutions USA Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1424-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 20 February 2017 |
| EAN / barcode | 10249555 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The mobile-specific instructions was not shipped to a limited population of Biograph Mobile systems.
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 Siemens Medical Solutions USA 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.