Device recall
Z-1713-2017: NucliSENS Lysis Buffer, REF 200292 NucliSENS Lysis Buffer is intended to be use…
FDA device recall · Class II · BioMerieux SA
Key facts
| Recall number (Z-number) | Z-1713-2017 |
|---|---|
| Recall event | 76675 |
| Product | NucliSENS Lysis Buffer, REF 200292 NucliSENS Lysis Buffer is intended to be use for the release of total nucleic acid from biological specimens |
| Product code | PPM |
| Recalling firm | BioMerieux SA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2020 |
| 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