Device recall
Z-2257-2023: MEGADYNE Suction Coagulators, Product Code 004125 (Suction Coagulator…
FDA device recall · Class II · Megadyne Medical Products, Inc.
Key facts
| Recall number (Z-number) | Z-2257-2023 |
|---|---|
| Recall event | 92456 |
| Product | MEGADYNE Suction Coagulators, Product Code 004125 (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm)), Product Code 004225 (Suction Coagulator, Handswitching, 8 Fr, 6 inch (15.24cm), Product Code 004325 (Suction Coagulator, Handswitching, 12 Fr, 6 inch (15.24cm)), and Product Code 0041BN… |
| Product code | GEI |
| Recalling firm | Megadyne Medical Products, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K072559 |
| 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