GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
3 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (3)
- Inspections (1)
Devices registered here (1)
- Needle, Hypodermic, Single LumenProduct code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570
Recalls & enforcement
- Class IIOngoing2017-09-22Leaks complaints.
- Class IIOngoing2017-09-22Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
- Class IIOngoing2016-10-19Complaints about the needle is not smooth, with discoloration, a kind of gel agglomeration on the needle tip.
FDA inspections (1)
- VAI2017-11-30Voluntary Action Indicated · Compliance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
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. “GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD. (FEI 3008449424) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008449424-guangzhou-improve-medical-instruments-co/
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