Device recall
Z-0683-2025: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog Number…
FDA device recall · Class I · Nova Biomedical Corporation
Key facts
| Recall number (Z-number) | Z-0683-2025 |
|---|---|
| Recall event | 95783 |
| Product | StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog Number: 63910. Prescription use blood glucose ketone meter for near-patient testing |
| Recalling firm | Nova Biomedical Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1219029 |
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