MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)
FDA device recall Z-0940-2026 · posted 2025-12-18 · Open, Classified
Recall details
- Recalling firm
- PATH
- Reason for recall
- 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.
- Action taken
- On November 6, 2025 URGENT: MEDICAL DEVICE Field Corrective Action letters were sent to their two distributors. Actions to be taken: - Users will be asked to confirm the DPOAE protocol in use. - Verify the DPOAE Protocol used is not affected by the issue (DP1, DP2, DP3, DP4, DP17, DP18, DP19, DP20, DP21). - If any other protocol is used, please replace it by using AccuLink Software. Follow instructions in IFU to do so. - Remove all affected protocols (DP5-DP16) using AccuLink Software. Follow instructions in IFU to do so. - Complete and return the attached form to confirm these steps were followed. - The expected lifetime of the probes is two years from date of manufacture. Please put the products out of use, once this is reached.
- Root cause
- Component change control
- Status
- Open, Classified
- Product code
- GWJ
- Distribution
- Domestic: WI. International: Ireland.
- Date initiated
- 2025-11-06
- Date posted
- 2025-12-18
- Location
- Germering, Germany
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| EARPROBE (K100661) | Path Medical GmbH | 2010-07-01 |