Device recall
Z-0933-04: AMPLICOR HPV Master Mix Analyte Specific Reagent (HPV MMX), Catalog number…
FDA device recall · Class II · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0933-04 |
|---|---|
| Recall event | 28739 |
| Product | AMPLICOR HPV Master Mix Analyte Specific Reagent (HPV MMX), Catalog number 03582841190. |
| 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