Device recall
Z-1216-2007: LX125 Swivel Collimator, Model D800; Manual Radiographic Collimator; Summit…
FDA device recall · Class II · Summit Industries Inc.
Key facts
| Recall number (Z-number) | Z-1216-2007 |
|---|---|
| Recall event | 38512 |
| Product | LX125 Swivel Collimator, Model D800; Manual Radiographic Collimator; Summit Industries, Inc., Chicago, Illinois |
| Product code | IZX |
| Recalling firm | Summit Industries Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 18, 2010 |
| 510(k) numbers | K874687 |
| FEI number | 1450503 |
At a glance
- 1–9 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