[Recalled] Biograph 64-3R TruePoint w/ TrueV, Model Number 10097301 — Emission computed tomography systems and computed tomography xray systems with… | FDA 2015-07-14
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Biograph 64-3R TruePoint w/ TrueV, Model Number 10097301 |
|---|---|
| Brand / manufacturer | Siemens Medical Solutions USA Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2338-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 14 July 2015 |
| EAN / barcode | 10097301 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Emission computed tomography systems and computed tomography xray systems with optional ceiling mounts may be missing a locking ring.
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.