Device recall
Z-0101-2010: WA 1000A with Blank Console Model: 900506x.
FDA device recall · Class II · Cooper Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0101-2010 |
|---|---|
| Recall event | 53436 |
| Product | WA 1000A with Blank Console Model: 900506x. |
| Product code | GEH |
| Recalling firm | Cooper Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2012 |
| 510(k) numbers | K803311 |
| FEI number | 1216677 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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