FDA Device recall Z-0403-2024
AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
- FDA Device
- Class II
- ongoing
- Published 2023-12-06
On 2023-12-06 the FDA classified a Class II recall of AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP by Path, citing affected lots of product may experience technical distortions to a greater extent than expected.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0403-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-26 |
| Published | 2023-12-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Path |
| Distribution | FL, MO, OH, WI |
Product
AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
Reason
Affected lots of product may experience technical distortions to a greater extent than expected.
Identifiers
| code_info | UDI-DI: 04260223143298; Serial Numbers: 260446-260468 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0403-2024%22
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