Device recall
Z-1658-2009: Celex/GE Precision MPi, REF no.: 02980000 Is an all-digital multipurpose tilt-C…
FDA device recall · Class II · NRT - Nordisk Rontgen Teknik A/S
Key facts
| Recall number (Z-number) | Z-1658-2009 |
|---|---|
| Recall event | 52173 |
| Product | Celex/GE Precision MPi, REF no.: 02980000 Is an all-digital multipurpose tilt-C X-ray system, intended for a multitude of diagnostic procedures, including: R&F, radiology, fluoroscopy, interventional procedures, vascular and non-vascular procedures, and specialized applications including… |
| Product code | JAA |
| Recalling firm | NRT - Nordisk Rontgen Teknik A/S |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2009 |
| 510(k) numbers | K033486 |
| FEI number | 1000188474 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database