HANGZHOU ACOSOUND TECHNOLOGY CO., LTD.
1 recall(s) on record — most severe on record: Class III.
Activity by year
- Recalls (1)
Devices registered here (1)
- Hearing Aid, Air-Conduction With Wireless Technology, PrescriptionProduct code OSM (opens in a new tab) · Class II · Ear, Nose, Throat · 21 CFR 874.3305
Recalls & enforcement
- Class IIIOngoing2025-04-25Three 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 …
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “HANGZHOU ACOSOUND TECHNOLOGY CO., LTD. (FEI 3011350813) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011350813-hangzhou-acosound-technology-co-ltd/
Alerts for HANGZHOU ACOSOUND TECHNOLOGY CO., LTD.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.