Device recall
Z-1142-03: Abbott Aeroset System list number 9D05-01, manufactured by Abbott Diagnostic…
FDA device recall · Class III · Abbott Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-1142-03 |
|---|---|
| Recall event | 26640 |
| Product | Abbott Aeroset System list number 9D05-01, manufactured by Abbott Diagnostic Division, Irving, Texas |
| Product code | JJE |
| Recalling firm | Abbott Laboratories, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 20, 2003 |
| 510(k) numbers | K980367 |
| FEI number | 1628664 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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