Device recall
Z-0988-2007: MediSpectra Luma Cervical Imaging System Model Number: 3-02600
FDA device recall · Class III · Medispectra Inc.
Key facts
| Recall number (Z-number) | Z-0988-2007 |
|---|---|
| Recall event | 37954 |
| Product | MediSpectra Luma Cervical Imaging System Model Number: 3-02600 |
| Product code | MWM |
| Recalling firm | Medispectra Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 9, 2007 |
| PMA numbers | P040028 |
| FEI number | 3002634893 |
At a glance
- None 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