Device recall
Z-2320-2019: ABL90 FLEX Analyzer REF 393090 UDI:05700693930909
FDA device recall · Class II · Radiometer America Inc
Key facts
| Recall number (Z-number) | Z-2320-2019 |
|---|---|
| Recall event | 83312 |
| Product | ABL90 FLEX Analyzer REF 393090 UDI:05700693930909 |
| Product code | CEM |
| Recalling firm | Radiometer America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2022 |
| 510(k) numbers | K092686 |
| FEI number | 3010420736 |
At a glance
- 1–9 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