Device recall
Z-0066-04: Bayer Rapidpoint 405 Blood Gas Analyzer
FDA device recall · Class II · Bayer Corp.
Key facts
| Recall number (Z-number) | Z-0066-04 |
|---|---|
| Recall event | 27414 |
| Product | Bayer Rapidpoint 405 Blood Gas Analyzer |
| Product code | CHL |
| Recalling firm | Bayer Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2004 |
| 510(k) numbers | K020616 |
| FEI number | 3002637618 |
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