Recall archive / FDA company announcement
Ethicon Megadyne: Mega Soft Pediatric Patient Return Electrode — FDA announcement May 10, 2024
Published notice; closure not supplied
A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.
Source date May 10, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Mega Soft Pediatric Patient Return Electrode
- Reason
- Reports of patient burn injuries
- Classification
- Not supplied
- Recalling firm
- Megadyne Medical Products Inc.
- Quantity
- Not supplied
- Agency-reported status
- Company recall announcement
- Source record identifier
- f70f163eafa15607
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product Name | Product Code | UDI-DI; MEGADYNE™ MEGA SOFT™ Pediatric Patient Return Electrode | 0840 | 10614559103395 |
Match all identifying details in the current notice. A brand name alone is not enough.
Product tables from the announcement
These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.
| Product Name | Product Code | UDI-DI |
|---|---|---|
| MEGADYNE™ MEGA SOFT™ Pediatric Patient Return Electrode | 0840 | 10614559103395 |
Announcement retrieved Oct 1, 2026. Official announcement.
Distribution
Not supplied
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Fda listing date
- May 10, 2024
- Company announcement date
- May 10, 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.