Device recall
Z-2476-2019: cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
FDA device recall · Class II · Roche Diagnostics Operations, Inc.
Key facts
| Recall number (Z-number) | Z-2476-2019 |
|---|---|
| Recall event | 83525 |
| Product | cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001 |
| Product code | JJE |
| Recalling firm | Roche Diagnostics Operations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 15, 2020 |
| 510(k) numbers | K060373 |
| FEI number | 1823260 |
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