Device recall
Z-0459-2009: Sun Med GreenLine/D Laryngoscope Blades Compatible with Fiber Optic Green System…
FDA device recall · Class I · Sun Med, Inc.
Key facts
| Recall number (Z-number) | Z-0459-2009 |
|---|---|
| Recall event | 50092 |
| Product | Sun Med GreenLine/D Laryngoscope Blades Compatible with Fiber Optic Green System Handles, Sterile Disposable. Contents 20. |
| Product code | CCW |
| Recalling firm | Sun Med, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 6, 2010 |
| FEI number | 1314417 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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