FDA Recall Open, Classified

SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098

Recall: Z-0401-2024 · Initiated September 26, 2023

Recall

Recall Number
Z-0401-2024
Event Number
93275
Firm
PATH Landsberger Str. 65 Germering Germany
FEI Number
3008111228
Product Code
EWO
Status
Open, Classified
Root Cause
Process change control
Initiated
September 26, 2023
Posted
November 25, 2023

Description

SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098

Reason

Affected lots of product may experience technical distortions to a greater extent than expected.

Action

An URGENT: MEDICAL DEVICE RECALL SENTIERO notification letter dated 9/26/23 was sent to customers. Actions to be taken by the User: The technical distortions can influence the specified performance of the device when performing diagnostic DPOAEs at high stimuli. Therefore, PATH MEDICAL chose to voluntarily recall affected products for correction. 1. Immediately identify any affected devices at your location and quarantine them. 2. Please return your affected device(s) to your local distributor or PATH MEDICAL directly (Shipping Address: Landsberger Str. 65, 82110 Germering, Germany) to have your PCB replaced. Upon request, return labels can be provided. 3. If the device(s) have been further distributed to other accounts, please forward this notice to them to inform them of the recall. 4. Report any adverse events to FDA MedWatch: Use the MedWatch Online Reporting Form or call 800-332-1088. Re-Screening of patients screened with a device subject to the recall is not necessary, as regular DPAOE screening would not be done at stimuli as high as they would be affected by the issue. Furthermore, DPOAE-based hearing screening always consists of measurements at multiple frequencies. Therefore, false positive DPOAE detections at a single frequency, which are already considered unlikely, would not necessarily falsify the overall screening result (e.g., pass criterion 3 out of 4). Please be aware that your local competent authority may have been informed of this recall, if required by law. Thank you for your cooperation. In case there are additional questions, please contact us under: Mail: [email protected] Phone: +49 (0)89 80076502

Distribution

US States: FL, MO, OH, WI

Quantity

15 units