Device recall
Z-2324-2009: Sensititre Mueller-Hinton Broth w/Lysed Horse Blood (MHB w/LHB), Model Number…
FDA device recall · Class III · Trek Diagnostic Systems
Key facts
| Recall number (Z-number) | Z-2324-2009 |
|---|---|
| Recall event | 52813 |
| Product | Sensititre Mueller-Hinton Broth w/Lysed Horse Blood (MHB w/LHB), Model Number: CP112-10; Lot number 150444SA. In vitro diagnostic products for clinical susceptibility testing of H. influenzae and Streptococcus spp., can provide both qualitative and quantitative results. |
| Product code | JTZ |
| Recalling firm | Trek Diagnostic Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 26, 2010 |
| 510(k) numbers | K860753 |
| FEI number | 1000515493 |
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