PlainRecalls
FDA Devices Low Class III Ongoing

AcoSound. Model Number: LW12-BTE-M

Reported: June 25, 2025 Initiated: April 25, 2025 #Z-1976-2025

Product Description

AcoSound. Model Number: LW12-BTE-M

Reason for Recall

Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer's name is mislabeled as "Developed by AcoSound," Correct should be "Manufactured by Hangzhou AcoSound." And the labeling has no statement of the place of business for the manufacturer. 2. Customer information: The customer "Blaid" information is not correctly marked; Blaid is not the manufacturer. 3. UDI Information: The UDI information is incomplete and without DI information and correct Pl information, not complied with UDI label requirements.

Details

Units Affected
120 units
Distribution
US Nationwide distribution in the state of New York.
Location
Hangzhou, N/A

Frequently Asked Questions

What product was recalled?
AcoSound. Model Number: LW12-BTE-M. Recalled by HANGZHOU ACOSOUND TECHNOLOGY CO., LTD.. Units affected: 120 units.
Why was this product recalled?
Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer's name is mislabeled as "Developed by AcoSound," Correct should be "Manufactured by Hangzhou AcoSound." And the labeling has no statement of the place of business for the manufacturer. 2. Customer information: The customer "Blaid" information is not correctly marked; Blaid is not the manufacturer. 3. UDI Information: The UDI information is incomplete and without DI information and correct Pl information, not complied with UDI label requirements.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 25, 2025. Severity: Low. Recall number: Z-1976-2025.