---
title: "MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Retur... — FDA record Z-1920-2024 | Is It on Recall"
description: "Reports of patient burns."
url: https://isitonrecall.com/recall/fda-device-z-1920-2024-megadyne-mega-soft-pediatric-patient-return-electrode-reusable-patient-return-electrode-for-patients/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb... — FDA record Z-1920-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 8, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.
- **Reason**: Reports of patient burns.
- **Classification**: Class I
- **Recalling firm**: Megadyne Medical Products, Inc.
- **Quantity**: 1270
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1920-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1920-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model Number: 0840; UDI-DI: 10614559103395; Lot Number: All distributed lot numbers. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution. US nationwide including Puerto Rico; Australia, Austria, Bahrain, Belgium, Canada, Chile, Czechia, France, Germany, Greece, Hong Kong, India, Ireland, Italy, Japan, the Netherlands, Norway, Poland, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Switzerland, Thailand, United Arab Emirates, and United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jun 12, 2024
- **Recall initiation date**: May 8, 2024
- **Center classification date**: Jun 6, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1920-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Megadyne Medical Products, Inc. records](https://isitonrecall.com/brand/megadyne-medical-products-inc/)
