Device recall
Z-0721-03: AEROSET System Software version 1.00ER005 Catalog Number 2-89996-01 and…
FDA device recall · Class III · Abbott Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-0721-03 |
|---|---|
| Recall event | 25236 |
| Product | AEROSET System Software version 1.00ER005 Catalog Number 2-89996-01 and 1.00ER005.2 Catalog Number 2-89996-02, distributed by Abbott Laboratories |
| Product code | JJE |
| Recalling firm | Abbott Laboratories, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 28, 2004 |
| FEI number | 1628664 |
At a glance
- None 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