Device recall
Z-0669-2009: HARDY DIAGNOSTIC McFarland Standard 0.5; in vitro diagnostic, glass vial, one…
FDA device recall · Class II · Trek Diagnostic Systems
Key facts
| Recall number (Z-number) | Z-0669-2009 |
|---|---|
| Recall event | 50129 |
| Product | HARDY DIAGNOSTIC McFarland Standard 0.5; in vitro diagnostic, glass vial, one vial per box |
| Product code | JTZ |
| Recalling firm | Trek Diagnostic Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2010 |
| FEI number | 1000515493 |
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