Device recall
Z-1661-2015: Direct Water feed Kit, Catalog#10373222
FDA device recall · Class II · Siemens Medical Solutions Diagnostics
Key facts
| Recall number (Z-number) | Z-1661-2015 |
|---|---|
| Recall event | 71022 |
| Product | Direct Water feed Kit, Catalog#10373222 |
| Product code | JJE |
| Recalling firm | Siemens Medical Solutions Diagnostics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 16, 2018 |
| PMA numbers | P010053, P010053S007 |
| FEI number | 1000122204 |
At a glance
- None 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