Device recall
Z-0024-05: Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro…
FDA device recall · Class III · Remel, Inc.
Key facts
| Recall number (Z-number) | Z-0024-05 |
|---|---|
| Recall event | 30154 |
| Product | Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS. |
| Product code | KZI |
| Recalling firm | Remel, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 25, 2006 |
| FEI number | 1924669 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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