Device recall
Z-0086-2018: NucliSENS Lysis Buffer Extended lot for RES 76675
FDA device recall · Class II · BioMerieux SA
Key facts
| Recall number (Z-number) | Z-0086-2018 |
|---|---|
| Recall event | 78387 |
| Product | NucliSENS Lysis Buffer Extended lot for RES 76675 |
| Product code | PPM |
| Recalling firm | BioMerieux SA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2021 |
| FEI number | 1000611339 |
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