Device recall
Z-3213-2011: Crystal Metal Miller Disposable Blades (sizes 0 art no: 50676 and 00 part no…
FDA device recall · Class II · Penlon, Ltd. (Fmly East Healthcare)
Key facts
| Recall number (Z-number) | Z-3213-2011 |
|---|---|
| Recall event | 58820 |
| Product | Crystal Metal Miller Disposable Blades (sizes 0 art no: 50676 and 00 part no 50647 Disposable laryngoscope blades |
| Product code | CCW |
| Recalling firm | Penlon, Ltd. (Fmly East Healthcare) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 21, 2012 |
| FEI number | 3002807907 |
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