Device recall
Z-2642-2011: ONCOR Avant Garde, camera imaging system, Part Number:5863472; Product is…
FDA device recall · Class II · Siemens Medical Solutions USA, Inc - Radiation Oncology
Key facts
| Recall number (Z-number) | Z-2642-2011 |
|---|---|
| Recall event | 58813 |
| Product | ONCOR Avant Garde , camera imaging system, Part Number:5863472; Product is manufactured and distributed by SIEMENS MEDICAL SOLUTIONS USA, INC. Concord, CA; and SIEMENS AG, MEDICAL SOLUTIONS Roentgenstrasse, Kemnath, GERMANY, and SIEMENS AG, MEDICAL SOLUTIONS Henkestrasse, Erlangen, GERMANY The… |
| Product code | IYE |
| Recalling firm | Siemens Medical Solutions USA, Inc - Radiation Oncology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2011 |
| 510(k) numbers | K031764 |
| FEI number | 2937457 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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