Path recalls
Path appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2025-12-24.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 5 |
|---|---|
| Published | 2023-12-06 to 2025-12-24 |
| By agency | FDA Device (5) |
| By classification | Class II (5) |
| By status | ongoing (5) |
| Distribution named in notices | FL, MO, OH, WI |
Recalls
- MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)
FDA Device · Class II · 2025-12-24 · Path
Reason: 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… - SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S
FDA Device · Class II · 2023-12-06 · Path
Reason: Affected lots of product may experience technical distortions to a greater extent than expected. - SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098
FDA Device · Class II · 2023-12-06 · Path
Reason: Affected lots of product may experience technical distortions to a greater extent than expected. - SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2
FDA Device · Class II · 2023-12-06 · Path
Reason: Affected lots of product may experience technical distortions to a greater extent than expected. - AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
FDA Device · Class II · 2023-12-06 · Path
Reason: Affected lots of product may experience technical distortions to a greater extent than expected.