Device recall
Z-0725-04: VITEK GPS-106 Gram Positive Susceptibility Card, Catalog #V4335, for in-vitro…
FDA device recall · Class II · bioMerieux Inc
Key facts
| Recall number (Z-number) | Z-0725-04 |
|---|---|
| Recall event | 28429 |
| Product | VITEK GPS-106 Gram Positive Susceptibility Card, Catalog #V4335, for in-vitro diagnostic use, 20 cards per package. The responsible firm on the label is bioMerieux, Inc., Durham, NC and bioMerieux sa, France. |
| Product code | LON |
| Recalling firm | bioMerieux Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 24, 2004 |
| FEI number | 1950204 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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