Device recall
Z-0469-03: Megadyne MegaTip, Modified E-Z Clean Non Stick Cautery Tip, CAT/REF 0600M…
FDA device recall · Class II · Megadyne Medical Products, Inc
Key facts
| Recall number (Z-number) | Z-0469-03 |
|---|---|
| Recall event | 25265 |
| Product | Megadyne MegaTip, Modified E-Z Clean Non Stick Cautery Tip, CAT/REF 0600M, Single Use Only, STERILE |
| Product code | GEI |
| Recalling firm | Megadyne Medical Products, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 5, 2003 |
| 510(k) numbers | K943055 |
| FEI number | 1721194 |
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