MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
Reported: July 5, 2023 Initiated: June 1, 2023 #Z-1997-2023
Product Description
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
Reason for Recall
Firm has received reports of patient burns in surgical procedures where device was used.
Details
- Recalling Firm
- Megadyne Medical Products, Inc.
- Units Affected
- 21,100 units
- Distribution
- Distributed US Nationwide.
- Location
- Blue Ash, OH
Frequently Asked Questions
What product was recalled? ▼
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery. Recalled by Megadyne Medical Products, Inc.. Units affected: 21,100 units.
Why was this product recalled? ▼
Firm has received reports of patient burns in surgical procedures where device was used.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 5, 2023. Severity: Critical. Recall number: Z-1997-2023.
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