KONICA MINOLTA, INC.
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (3)
- KONICA MINOLTA TECHNOPRODUCTS CO., LTD. FEI 3005406110 · JP
- KONICA MINOLTA, INC. FEI 3004485675 · JP
- KONICA MINOLTA, INC. FEI 3003769120 · JP
Recalls & enforcement
- Class IITerminated2017-04-24The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.
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. “KONICA MINOLTA, INC. — 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-9009884-konica-minolta-inc/
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