Konica Minolta Healthcare Americas, Inc.
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (1)
- Konica Minolta Healthcare Americas, Inc FEI 3002885429 · NC
Recalls & enforcement
- Class IITerminated2021-12-03lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel potential risk of incorrect length measurement/area calculation if incorrect power sequence is followed
- Class IITerminated2018-11-08Unintentional U-Arm movement
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 Healthcare Americas, 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-2241281-konica-minolta-healthcare-americas-inc/
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