Device recall
Z-0797-2023: VIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226
FDA device recall · Class II · Biomerieux Inc
Key facts
| Recall number (Z-number) | Z-0797-2023 |
|---|---|
| Recall event | 91148 |
| Product | VIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226 |
| Product code | LYR |
| Recalling firm | Biomerieux Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K141133 |
| FEI number | 1950204 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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