ZHEJIANG LUYAO ELECTRONICS TECHNOLOGY CO.,LTD
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (1)
- Massager, Powered Inflatable TubeProduct code IRP (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5650
Recalls & enforcement
- Class IIOngoing2025-01-17Regulatory documentation error and misleading color packaging claim.
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. “ZHEJIANG LUYAO ELECTRONICS TECHNOLOGY CO.,LTD (FEI 3009942828) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009942828-zhejiang-luyao-electronics-technology-co/
Alerts for ZHEJIANG LUYAO ELECTRONICS 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.