NIKKISO CO., LTD.
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (5)
- NIKKISO CO., LTD. - SHIZUOKA PLANT FEI 3002807721 · JP
- M. E. NIKKISO CO., LTD. FEI 3008229990 · TH
- M.E.Nikkiso Vietnam Co., Ltd. FEI 3027859369 · VN
- NIKKISO CO., LTD. FEI 3014638255 · JP
- NIKKISO CO., LTD. KANAZAWA PLANT FEI 3040314808 · JP
Recalls & enforcement
- Class IIOngoing2021-11-24Device lacks premarket approval.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “NIKKISO CO., LTD. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-8031561-nikkiso-co-ltd/
Alerts for NIKKISO 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.