FDA Devices recall · Reported June 25, 2025
AcoSound. Model Number: LW12-BTE-M
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 "Ma…
Hangzhou Acosound Technology CO., LTD. recalled AcoSound. Model Number: LW12-BTE-M - a low-severity action.
AcoSound. Model Number: LW12-BTE-M was recalled by Hangzhou Acosound Technology CO., LTD. in June 25, 2025. Reason: Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer'…. Check the official notice for the remedy. Verify recall #Z-1976-2025 with the FDA Devices before acting.
The recall
Hangzhou Acosound Technology CO., LTD. issued this low-severity FDA Devices recall-Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer'….
- Low
- severity level
- 120 units
- affected scope
- Class III
- classification
- June 25, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1976-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 41,021 medical devices recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Ongoing |
| Recall number | Z-1976-2025 |
| Date reported | June 25, 2025 |
| Date initiated | April 25, 2025 |
| Recalling firm | Hangzhou Acosound Technology CO., LTD. |
| Firm location | Hangzhou, N/A |
| Affected scope | 120 units |
| Distribution | US Nationwide distribution in the state of New York. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1976-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Low), closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026