FDA Device recall Z-2792-2018
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
- FDA Device
- Class II
- terminated
- Published 2018-08-22
On 2018-08-22 the FDA classified a Class II recall of MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715 by Megadyne Medical Products, citing if two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the pati….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2792-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-15 |
| Published | 2018-08-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Megadyne Medical Products |
| Distribution | US |
Product
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
Reason
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient.
Identifiers
| code_info | 00001001 00010001 13806001 00053001 00063001 00066001 00070001 00078001 00085001 00091001 00100001 00105001…00001001 00010001 13806001 00053001 00063001 00066001 00070001 00078001 00085001 00091001 00100001 00105001 00110001 00115001 00128001 00132001 00146001 00167001 00181001 00187001 00191001 00200001 00211001 00212001 00223001 00229001 00237001 00240001 00242001 00246001 00248001 00254001 00265001 00278001 00282001 00283001 00308001 00313001 00313001 00314001 00333001 00334001 00379001 00380001 00391001 00398001 00402001 00413001 00416001 00418001 00424001 00432001 00437001 00438001 00458001 00459001 00471001 00479001 00481001 00484001 00524001 00535001 00543001 00551001 00553001 00554001 00574001 00586001 00590001 00619001 00627001 00632001 00638001 00639001 00640001 00658001 00685001 00690001 00693001 00707001 00708001 00710001 00721001 00725001 00728001 00731001 00740001 00779001 00796001 00801001 00804001 00813001 00816001 00829001 00841001 00847001 00848001 00859001 00868001 00871001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2792-2018%22
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