PATH Recalls
5 recalls on record · December 6, 2023 to December 24, 2025 · Medical Devices
Recalls by year
23
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 24, 2025Medical DevicesFDA
PATH recalls MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)
Hazard: Following a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude acceptance thresholds. These distortions can mimic true DPOAE responses and may result in a false PASS outcome.
December 6, 2023Medical DevicesFDA
PATH recalls SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S
Hazard: Affected lots of product may experience technical distortions to a greater extent than expected.
December 6, 2023Medical DevicesFDA
PATH recalls AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
Hazard: Affected lots of product may experience technical distortions to a greater extent than expected.
December 6, 2023Medical DevicesFDA
PATH recalls SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2
Hazard: Affected lots of product may experience technical distortions to a greater extent than expected.
December 6, 2023Medical DevicesFDA
PATH recalls SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098
Hazard: Affected lots of product may experience technical distortions to a greater extent than expected.