# FDA recall Z-2792-2018

> **Megadyne Medical Products, Inc.** · Class II · device recall initiated 2018-05-15.

## 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.

## Distribution

Worldwide distribution.  US Nationwide, Mexico, Europe, Middle East, Latin America, Africa, and Asia Pacific Markets

## Key facts

- **Recall number:** Z-2792-2018
- **Recalling firm:** Megadyne Medical Products, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-15
- **Report date:** 2018-08-22
- **Termination date:** 2024-01-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Draper, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2792-2018

## Citation

> AI Analytics. FDA recall Z-2792-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2792-2018. Source: US FDA. Licensed CC0.

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