Device recall
Z-0657-03: Hybrid Capture II CT-ID Test, Catalog #5135-1050IVT, (labeled for export only).
FDA device recall · Class II · Digene Corp
Key facts
| Recall number (Z-number) | Z-0657-03 |
|---|---|
| Recall event | 25678 |
| Product | Hybrid Capture II CT-ID Test, Catalog #5135-1050IVT, (labeled for export only). |
| Product code | MAQ |
| Recalling firm | Digene Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 16, 2003 |
| 510(k) numbers | K990023 |
| FEI number | 3003572099 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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