Device recall
Z-1451-06: BHI Agar with Vancomycin, for in vitro diagnostic use. Catalog # G14, Lot# 06136
FDA device recall · Class III · Hardy Media Inc Dba Hardy Diag
Key facts
| Recall number (Z-number) | Z-1451-06 |
|---|---|
| Recall event | 36048 |
| Product | BHI Agar with Vancomycin, for in vitro diagnostic use. Catalog # G14, Lot# 06136 |
| Product code | JSO |
| Recalling firm | Hardy Media Inc Dba Hardy Diag |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 14, 2011 |
| 510(k) numbers | K964560 |
| FEI number | 2022807 |
At a glance
- 1–9 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