Device recall
Z-0660-05: IMx HAVAB Controls In Vitro Test
FDA device recall · Class III · Abbott Health Products, Inc.
Key facts
| Recall number (Z-number) | Z-0660-05 |
|---|---|
| Recall event | 31342 |
| Product | IMx HAVAB Controls In Vitro Test |
| Product code | LOL |
| Recalling firm | Abbott Health Products, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 29, 2005 |
| PMA numbers | P780012, P780012S007 |
| FEI number | 2623532 |
At a glance
- None 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