Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K080741 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patien... | 1 | 07/03/2024 |
FEI # 1721194 Megadyne Medical Products, Inc. |
| MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patient... | 1 | 06/06/2024 |
FEI # 1721194 Megadyne Medical Products, Inc. |
| MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery | 1 | 06/30/2023 |
FEI # 1721194 Megadyne Medical Products, Inc. |
-







