Health & Personal Care
HIGH
FDA DEVICE
DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)
DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.
DERMASENSOR
Potential for