Device recall
Z-0934-04: AMPLICOR HPV Microwell Plate Analyte Specific Reagent (MWP); catalog…
FDA device recall · Class II · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0934-04 |
|---|---|
| Recall event | 28739 |
| Product | AMPLICOR HPV Microwell Plate Analyte Specific Reagent (MWP); catalog 03579229190. |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2005 |
| FEI number | 1823260 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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