Device recall
Z-0422-2022: RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4…
FDA device recall · Class II · Biomerieux Inc
Key facts
| Recall number (Z-number) | Z-0422-2022 |
|---|---|
| Recall event | 89041 |
| Product | RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD. |
| Product code | JSS |
| Recalling firm | Biomerieux Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2025 |
| FEI number | 1950204 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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