Device recall
Z-1032-2016: PINPOINT Endoscopic Fluorescence Imaging System
FDA device recall · Class II · Novadaq Technologies Inc.
Key facts
| Recall number (Z-number) | Z-1032-2016 |
|---|---|
| Recall event | 73225 |
| Product | PINPOINT Endoscopic Fluorescence Imaging System |
| Product code | GCJ |
| Recalling firm | Novadaq Technologies Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2016 |
| 510(k) numbers | K091515 |
| FEI number | 3012345110 |
At a glance
- 1–9 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