Device recall
Z-0743-2007: Mega Diagnostics Ammonia/Alcohol Controls (Cat.# A7504-CTL) packaged in 5ml…
FDA device recall · Class III · Mega Diagnostics
Key facts
| Recall number (Z-number) | Z-0743-2007 |
|---|---|
| Recall event | 37254 |
| Product | Mega Diagnostics Ammonia/Alcohol Controls (Cat.# A7504-CTL) packaged in 5ml vials |
| Product code | JIX |
| Recalling firm | Mega Diagnostics |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 4, 2012 |
| 510(k) numbers | K972333 |
| FEI number | 3008094524 |
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