Device recall
Z-1068-2010: CHROMagar 0157; 5000 ml (29.2 g/L) EE222; IVD For In Vitro Diagnostic Use…
FDA device recall · Class II · DRG International Inc
Key facts
| Recall number (Z-number) | Z-1068-2010 |
|---|---|
| Recall event | 53841 |
| Product | CHROMagar 0157; 5000 ml (29.2 g/L) EE222; IVD For In Vitro Diagnostic Use, CHROMagar is a trademark of Dr. A. Rambach; CHROMagar, Paris France. Medium for the detection of Van A Van B VRE. The majority of customers use this product for food, environmental, research or veterinarian use. |
| Product code | JSO |
| Recalling firm | DRG International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 14, 2012 |
| FEI number | 2245285 |
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