Device recall
Z-2779-2016: VIDAS NT-pro-BNP Product Usage: VIDAS NTproBNP (PBNP) is an automated…
FDA device recall · Class III · Biomerieux France Chemin De L'Or
Key facts
| Recall number (Z-number) | Z-2779-2016 |
|---|---|
| Recall event | 73989 |
| Product | VIDAS NT-pro-BNP Product Usage: VIDAS NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked… |
| Product code | NBC |
| Recalling firm | Biomerieux France Chemin De L'Or |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 21, 2017 |
| 510(k) numbers | K073091 |
| FEI number | 1000611339 |
At a glance
- 1–9 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