Device recall
Z-0167-2007: Data Innovations Instrument Manager Version 8:00, 8.01, 8.02, 8.03 or 8.04 with…
FDA device recall · Class II · Data Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-0167-2007 |
|---|---|
| Recall event | 36508 |
| Product | Data Innovations Instrument Manager Version 8:00, 8.01, 8.02, 8.03 or 8.04 with Specimen Management and using Results/Edit/ReleaseScreen (R/E/R) |
| Product code | JQP |
| Recalling firm | Data Innovations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2016 |
| FEI number | 3001451449 |
At a glance
- None Linked 510(k)s
- 1–9 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