Device recall
Z-0979-2010: Oxoid CM0225 Brain Heart Infusion IVD. The firm name on the label is Oxoid Ltd…
FDA device recall · Class II · Remel, Inc
Key facts
| Recall number (Z-number) | Z-0979-2010 |
|---|---|
| Recall event | 54194 |
| Product | Oxoid CM0225 Brain Heart Infusion IVD. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. The product is used for the cultivation of streptococci, pneumococci, meningococci and other fastidious organisms and is suitable for blood culture work. |
| Product code | JSC |
| Recalling firm | Remel, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 12, 2011 |
| 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