Device recall
Z-2270-2023: Over-Head Ceiling Tube Support, CH-200, CH-200M, Used with RadSpeed and RadSpeed…
FDA device recall · Class II · SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Key facts
| Recall number (Z-number) | Z-2270-2023 |
|---|---|
| Recall event | 92391 |
| Product | Over-Head Ceiling Tube Support, CH-200, CH-200M, Used with RadSpeed and RadSpeed PRO, Sonial Vision safire, Versa and G4 units, FluoroSpeed 300 and X1 units |
| Product code | IYB |
| Recalling firm | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002808139 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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