Device recall
Z-0438-03: PO2 electrode for Roche AVL OMNI Analyzers. Catalog number BP1734.
FDA device recall · Class III · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0438-03 |
|---|---|
| Recall event | 25169 |
| Product | PO2 electrode for Roche AVL OMNI Analyzers. Catalog number BP1734. |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 19, 2003 |
| 510(k) numbers | K013373 |
| FEI number | 1823260 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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