Device recall
Z-0937-2009: MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared…
FDA device recall · Class II · Flir Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0937-2009 |
|---|---|
| Recall event | 51488 |
| Product | MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared laser for Laser Range Finding (LRF). |
| Product code | REQ |
| Recalling firm | Flir Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 2, 2015 |
| FEI number | 1220474 |
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