Device recall
Z-1045-04: Magnetic Resonance Imaging System(s) Visart and Exelart P2/ Exelart P3/ Exelart…
FDA device recall · Class II · Toshiba American Med Sys Inc
Key facts
| Recall number (Z-number) | Z-1045-04 |
|---|---|
| Recall event | 29226 |
| Product | Magnetic Resonance Imaging System(s) Visart and Exelart P2/ Exelart P3/ Exelart SPIN and Exelart VANTAGE |
| Product code | LNH |
| Recalling firm | Toshiba American Med Sys Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2005 |
| 510(k) numbers | K002531, K990620 |
| FEI number | 2020563 |
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