PlainRecalls

Philips North America

Compiled from official public sources by the publisher.

126 recalls on record · Latest: May 6, 2026

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Agency notice ledger

Federal filing book Philips North America HEAVY-BOOK · SINGLE-AGENCY

#127 of 14,151 · 126 notices · 0.121% archive

  • BOOK 126 notices
  • RANK #127 of 14,151
  • SHARE 0.121% archive
  • AGENCY FDA Devices (126)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 6, 2026
  • PHOTO Roche Diagnostics Ope…

Nearest notice-volume peer: Roche Diagnostics Operations, Inc. (1 notice gap)

Philips North America accounts for about 0.121% of the 104,423-notice archive on 126 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Philips North America compares to 14,151 recalling firms

Philips North America ranks 127th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips North America vs all firms by recall-notice count

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

126 127th of 14151 higher than 14,024 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 · 2026-09-13

Philips North America in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips North America holds about 0.121% of archive notices alongside 126 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 17, 2024

(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)
FDA Devices Moderate Jan 17, 2024

BrightView, Gamma Camera System, Product Code 882480.
FDA Devices Moderate Jan 17, 2024

BrightView XCT, Gamma Camera, Product Code 882482
FDA Devices Moderate Nov 22, 2023

Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
FDA Devices Moderate Nov 22, 2023

Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
FDA Devices Moderate Nov 15, 2023

Allura Xper IGTS Fixed Systems
FDA Devices Moderate Nov 15, 2023

BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery C-arm systems.
FDA Devices Moderate Nov 15, 2023

Veradius Unity Mobile Surgery C-arm
FDA Devices Moderate Nov 15, 2023

Zenition 50 & 70 Mobile Surgery C-arm
FDA Devices Moderate Nov 15, 2023

Azurion IGTS Fixed Systems
FDA Devices Moderate Nov 15, 2023

Integris-Allura IGTS Fixed Systems
FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
FDA Devices Moderate Aug 16, 2023

Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
FDA Devices Moderate Aug 16, 2023

Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
FDA Devices Moderate Aug 9, 2023

Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
FDA Devices Moderate Aug 9, 2023

Incisive CT-Computed Tomography X-Ray System Model: 728143
FDA Devices Moderate Aug 9, 2023

Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148
FDA Devices Moderate Aug 9, 2023

Incisive CT Plus-Computed Tomography X-Ray System Model: 728149
FDA Devices Moderate May 24, 2023

ProxiDiagnost N90 R.1.0
FDA Devices Moderate May 24, 2023

CombiDiagnost R90 R.1.0
FDA Devices Moderate May 24, 2023

CombiDiagnost R90 R1.1
FDA Devices Moderate May 24, 2023

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
FDA Devices Moderate May 24, 2023

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814

Philips North America carries an outsized archive share

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (126 here — heavy-book).

Roche Diagnostics Operations, Inc. 127 Abbott Laboratories 124 Krs Global Biotechnology, Inc 129 Treehouse Foods 129 Pfizer Inc. 123

Similar medical devices volume

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

Roche Diagnostics Operations, Inc. 127 Abbott Laboratories 124 Covidien, LP 131 Philips Ultrasound, Inc 132

Frequently Asked Questions

How many federal recall notices name Philips North America? ▼
PlainRecalls indexes 126 distinct federal recall events naming Philips North America, 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 North America sit among other recalling firms? ▼
Philips North America ranks #127 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips North America's notices? ▼
FDA Devices accounts for 126 of this firm's 126 indexed notices.
What product category dominates Philips North America's filing book? ▼
Filings for Philips North America 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 North America: 126 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 North America; individual notices remain authoritative on each linked recall page.

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