PlainRecalls

Konica Minolta Healthcare Americas, Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jan 26, 2022

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Agency notice ledger

Federal filing book Konica Minolta Healthcare A… LIGHT-BOOK · SINGLE-AGENCY

#5,168 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,168 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 26, 2022
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Konica Minolta Healthcare Americas, Inc. accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Konica Minolta Healthcare A…'s standing among 14,151 recalling firms

Konica Minolta Healthcare Americas, Inc. ranks 5,168th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Konica Minolta Healthcare A… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

2 5168th of 14151 higher than 8,037 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-10-28

Konica Minolta Healthcare A… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Konica Minolta Healthcare Americas, Inc. holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Jan 26, 2022

ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medical diagnostics Product number: ADFR and ADJC
FDA Devices Moderate Dec 26, 2018

Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17; Board Name; Board Version, Firmware Version Advanced Universal U-Arm 4000 System. The Positioner consists of the following associated subassemblies: Vertical Column, Swivel Arm with variable height, X-ray Tube, Automatic Exposure Control, Collimator, Touch Screen Control and Image Receptor Assembly. The Positioner and the Patient Mobile Table are associated equipment to the Generator X-ray Unit.

Konica Minolta Healthcare A… is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Konica Minolta Healthcare A…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Konica Minolta Healthcare Americas, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Konica Minolta Healthcare A… sit among other recalling firms? ▼
Konica Minolta Healthcare Americas, Inc. ranks #5,168 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Konica Minolta Healthcare A…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Konica Minolta Healthcare A…'s filing book? ▼
Filings for Konica Minolta Healthcare Americas, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Konica Minolta Healthcare Americas, Inc.: 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Konica Minolta Healthcare Americas, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of October 2026