Health & Personal Care
HIGH
FDA DEVICE
Edermy Recalls Medical Devices Due to Lack of 510K Clearance
Edermy LLC recalled 11,202 medical devices on January 14, 2026. The recall affects models P2HC-A, P2HC-S, and P2HC due to lack of proper FDA clearance. Patients and healthcare providers should immediately cease use of these devices and follow recall instructions.
Edermy
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