Device recall
Z-0722-2007: Clinical Chemistry Phosphorus in vitro diagnostic, List Number: 7D71-30 and…
FDA device recall · Class II · Abbott Laboratories Inc.
Key facts
| Recall number (Z-number) | Z-0722-2007 |
|---|---|
| Recall event | 37334 |
| Product | Clinical Chemistry Phosphorus in vitro diagnostic, List Number: 7D71-30 and 7D71-20 |
| Product code | CEO |
| Recalling firm | Abbott Laboratories Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 10, 2011 |
| 510(k) numbers | K981759 |
| FEI number | 2018433 |
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