Device recall
Z-0733-2014: Consult Diagnostics Eon Calcium Reagent For In-Vitro Diagnostic Use PN: 1429 For…
FDA device recall · Class II · Vital Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-0733-2014 |
|---|---|
| Recall event | 66202 |
| Product | Consult Diagnostics Eon Calcium Reagent For In-Vitro Diagnostic Use PN: 1429 For the quantitative measurement of calcium in plasma and serum |
| Product code | CJY |
| Recalling firm | Vital Diagnostics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 26, 2015 |
| 510(k) numbers | K120626 |
| FEI number | 1717966 |
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