Device recall
Z-1201-2025: remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic…
FDA device recall · Class II · Remel, Inc
Key facts
| Recall number (Z-number) | Z-1201-2025 |
|---|---|
| Recall event | 96312 |
| Product | remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use |
| Product code | JSI |
| Recalling firm | Remel, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1924669 |
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