Megadyne Medical Products, Inc.: Medical Device Recalls in 2023
Updated on March 25, 2026.
According to to data from the FDA, there were 9 medical device recalls made by Megadyne Medical Products, Inc. in 2023. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery
- 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 (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm), Bulk Non Sterile)
- MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
- MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery