Device recall
Z-1177-2014: bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical…
FDA device recall · Class II · Biomerieux Inc
Key facts
| Recall number (Z-number) | Z-1177-2014 |
|---|---|
| Recall event | 67463 |
| Product | bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical Device), (REF 29500/29500R), bioMerieux, Hazelwood, MO. |
| Product code | LIB |
| Recalling firm | Biomerieux Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 16, 2017 |
| FEI number | 1950204 |
At a glance
- None 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