MegaPower Electrosurgical Generator — Class II medical device recall Z-2792-2018
Terminated recall by Megadyne Medical Products, Inc., reported 2018-08-22, distributed nationwide. If two devices are plugged into the same channel/port in the generator, both devices activate. If one device i
| Recall number | Z-2792-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Megadyne Medical Products, Inc., Draper, UT, United States |
| Recall initiated | 2018-05-15 |
| Classified | 2018-08-13 |
| Reported by FDA | 2018-08-22 |
| Terminated | 2024-01-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | MX |
| Quantity | 8,380 units |
| UPC / GTIN / UDI-DI | 10614559103715 |
Product
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2792-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.