Device recall
Z-0728-2008: Invictus-- Bionime Rightest Blood Glucose Monitoring System MODEL: GM300…
FDA device recall · Class III · Invictus Scientific Inc
Key facts
| Recall number (Z-number) | Z-0728-2008 |
|---|---|
| Recall event | 45953 |
| Product | Invictus-- Bionime Rightest Blood Glucose Monitoring System MODEL: GM300; Invictus Scientific, Inc., San Diego, CA |
| Product code | NBW |
| Recalling firm | Invictus Scientific Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 13, 2011 |
| 510(k) numbers | K042678, K053635, K062567 |
| FEI number | 3005498483 |
At a glance
- 1–9 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