Device recall
Z-1624-2008: Remel RapID Inoculation Fluid, Microorganism differentiation and identification…
FDA device recall · Class III · Remel Inc
Key facts
| Recall number (Z-number) | Z-1624-2008 |
|---|---|
| Recall event | 46801 |
| Product | Remel RapID Inoculation Fluid, Microorganism differentiation and identification device, Packaged in 1-ml tube, Catalog Number: R8325102, 20/pack, Remel, Lenexa, KS 66215 |
| Product code | LIB |
| Recalling firm | Remel Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 16, 2008 |
| 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