Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due to Manufacturing defects in devices manufactured from 4/1/25 to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lutronic Corporation directly.
Affected Products
XERF EFFECTOR 60. Electrosurgical unit.
Quantity: 7,490 units
Why Was This Recalled?
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lutronic Corporation
Lutronic Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report