Device recall
Z-0695-03: Cidex Plus Solution Test Strips
FDA device recall · Class III · Advanced Sterilization Products
Key facts
| Recall number (Z-number) | Z-0695-03 |
|---|---|
| Recall event | 25725 |
| Product | Cidex Plus Solution Test Strips |
| Product code | 6885 |
| Recalling firm | Advanced Sterilization Products |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 27, 2004 |
| 510(k) numbers | K981054 |
| FEI number | 3003662624 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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