[Recalled] ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model Number 10849000 — Temperature of the detector may fall out of its designed working range (cool do… | FDA 2018-07-29
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model Number 10849000 |
|---|---|
| Brand / manufacturer | Siemens Medical Solutions USA, Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-3190-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 29 July 2018 |
| EAN / barcode | 10849000 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Temperature of the detector may fall out of its designed working range (cool down) due to incorrectly configured temperature control unit. This unintentional system behavior may occur while the unit is powered down for long periods (e.g. at night).
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.