PlainRecalls

Philips Medical Systems

Compiled from official public sources by the publisher.

16 recalls on record · Latest: Aug 5, 2026

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Agency notice ledger

Federal filing book Philips Medical Systems LIGHT-BOOK · SINGLE-AGENCY

#992 of 14,151 · 16 notices · 0.015% archive

  • BOOK 16 notices
  • RANK #992 of 14,151
  • SHARE 0.015% archive
  • AGENCY FDA Devices (16)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 5, 2026
  • PHOTO Acella Pharmaceutical…

Nearest notice-volume peer: Acella Pharmaceuticals, LLC (0 notice gap)

Philips Medical Systems accounts for about 0.015% of the 104,423-notice archive on 16 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Philips Medical Systems sits among 14,151 recalling firms

Philips Medical Systems ranks 992nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips Medical Systems vs all firms by recall-notice count

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

16 992nd of 14151 higher than 13,145 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 · 2026-09-14

Philips Medical Systems in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Medical Systems holds about 0.015% of archive notices alongside 16 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 5, 2026

IQon Spectral CT IQon Spectral CT Upgrades
FDA Devices Moderate Aug 5, 2026

Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
FDA Devices Moderate Aug 5, 2026

Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium Ingenuity CT Upgrades Ingenuity CT China Ingenuity Core 128 Elite Brazil
FDA Devices Moderate Apr 22, 2026

Philips Spectral CT on Rails. Model Number: 728334.
FDA Devices Moderate Nov 5, 2025

Model: Incisive CT for Brazil SKD; Product Code (REF): 728146; Software Versions: 5.1.0.X & 5.1.1.X;
FDA Devices Moderate Nov 5, 2025

Model: CT 5300; Product Code (REF): 728285; Software Versions: 5.1.0.X & 5.1.1.X;
FDA Devices Moderate Nov 5, 2025

Model: Incisive CT; Product Code (REF): (1) 728143, (2) 728144; Software Versions: 5.1.0.X & 5.1.1.X;
FDA Devices Moderate Feb 21, 2024

CombiDiagnost R90 1.1 (709031)
FDA Devices Moderate Feb 21, 2024

CombiDiagnost R90 1.0 (709030)
FDA Devices Moderate Feb 14, 2024

Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.
FDA Devices Moderate Feb 14, 2024

Spectral CT on Rails: Software Version 5.1.0.X, model 728334.
FDA Devices Moderate Oct 12, 2016

Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Oct 12, 2016

Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Oct 12, 2016

Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Oct 12, 2016

Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Feb 10, 2016

DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621

Philips Medical Systems holds a measurable archive slice

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

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Cell Marque Corporation 16 Churchill Medical Systems, Inc. 16 Flower Orthopedics Corporation 16 Greatbatch Medical 16

Frequently Asked Questions

How many federal recall notices name Philips Medical Systems? ▼
PlainRecalls indexes 16 distinct federal recall events naming Philips Medical Systems, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Philips Medical Systems sit among other recalling firms? ▼
Philips Medical Systems ranks #992 of 14,151 by distinct recall-event count among 14,151 firms in this archive (93rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips Medical Systems's notices? ▼
FDA Devices accounts for 16 of this firm's 16 indexed notices.
What product category dominates Philips Medical Systems's filing book? ▼
Filings for Philips Medical Systems 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.
Philips Medical Systems: 16 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 Philips Medical Systems; individual notices remain authoritative on each linked recall page.

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