Device recall
Z-0870-2010: ERIC (Electronic RapID Compendium) Version 1.0.77, Catalog Number R8323600, used…
FDA device recall · Class III · Remel, Inc
Key facts
| Recall number (Z-number) | Z-0870-2010 |
|---|---|
| Recall event | 53800 |
| Product | ERIC (Electronic RapID Compendium) Version 1.0.77, Catalog Number R8323600, used in conjunction with: remel RapID Yeast Plus System is a qualitative micromethod employing conventional and chromogenic substrates for the identification of medically important yeast, yeast-like, and related organisms… |
| Product code | JXB |
| Recalling firm | Remel, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 3, 2010 |
| 510(k) numbers | K943621 |
| FEI number | 1924669 |
At a glance
- 1–9 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