Siemens Medical Solutions USA, Inc Recall: Siemens ARTIS pheno, Model # 10849000. Interven
Siemens Medical Solutions USA, Inc Recall: Siemens ARTIS pheno, Model # 10849000. Interven is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Siemens Medical Solutions USA, Inc; Product: Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angio
| Recalling firm | Siemens Medical Solutions USA, Inc |
|---|---|
| Product | Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. |
| Reason for recall | The potential exists for system movement to be permanently blocked by an activation of the collision sensor integrated in the cover of the collimator even when no collision has occurred. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide distribution in the states of FL, IL, IN, MA, PA, VA. |
| Recall initiated | 20191220 |
| Recall number | Z-0807-2020 |
| Category | device |
| State | PA |
| Country | United States |
$29/mo
Try RecallGuard →