MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)
FDA Recall Z-0940-2026 · Posted 2025-12-18
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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.
Firm Action
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
Distribution Pattern
Domestic: WI. International: Ireland.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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