Device recall
Z-1698-2011: The Waste Line Assembly and the Waste Outlet Tubing and the Waste Bottle Cable…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1698-2011 |
|---|---|
| Recall event | 54665 |
| Product | The Waste Line Assembly and the Waste Outlet Tubing and the Waste Bottle Cable are components that are used on one or more CELL-DYN Systems. Usage: Accessories to human waste container systems |
| Product code | GKZ |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 18, 2011 |
| 510(k) numbers | K030513, K870233, K951496, K972354, K980614, K991142 |
| FEI number | 2919069 |
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