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 Aug 6, 2025

Intera 3.0T Quasar Dual Model Number (REF): 781150;
FDA Devices Moderate Aug 6, 2025

Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
FDA Devices Moderate Aug 6, 2025

SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
FDA Devices Moderate Aug 6, 2025

MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
FDA Devices Moderate Aug 6, 2025

Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva Nova-Dual Product Number: 781173;
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Explorer/Nova Dual Product Number: 781108;
FDA Devices Moderate Jun 18, 2025

SmartPath to dStream for 1.5T¿; Product Number: 782146;
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva IT Nova Product Number: 781175
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva Nova Product Number: 781172;
FDA Devices Moderate Jun 18, 2025

Intera Achieva 1.5T Pulsar; Product Number: 781171;
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Master/Nova Product Number: 781106;
FDA Devices Moderate Jun 18, 2025

Intera 1.5T Omni/Stellar; Product Number: 781104;
FDA Devices Moderate Jun 18, 2025

Achieva XR Product Numbers: (1) 781153, (2) 781253;
FDA Devices Moderate Oct 16, 2024

Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
FDA Devices Moderate Oct 9, 2024

IntelliVue G7m Anesthesia Gas Module, Product Number 866173
FDA Devices Moderate Oct 2, 2024

IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 866064), and MX550 (Model Number 866066)
FDA Devices Moderate Apr 17, 2024

PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143
FDA Devices Moderate Apr 3, 2024

CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
FDA Devices Moderate Apr 3, 2024

Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
FDA Devices Moderate Feb 21, 2024

ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
FDA Devices Moderate Feb 21, 2024

ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
FDA Devices Critical Feb 14, 2024

BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2170-3002A 2170-3003A
FDA Devices Moderate Feb 14, 2024

Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Devices Critical Feb 14, 2024

BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161
FDA Devices Moderate Feb 14, 2024

Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Devices Critical Feb 14, 2024

BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;
FDA Devices Moderate Feb 14, 2024

Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
FDA Devices Moderate Feb 7, 2024

Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
FDA Devices Moderate Feb 7, 2024

SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129.
FDA Devices Moderate Feb 7, 2024

Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
FDA Devices Moderate Feb 7, 2024

Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
FDA Devices Moderate Feb 7, 2024

Achieva XR. Model (REF) Numbers 781153, 781253.
FDA Devices Moderate Feb 7, 2024

Achieva 1.5T Initial system. Model (REF) Numbers 781178.
FDA Devices Moderate Feb 7, 2024

Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
FDA Devices Moderate Feb 7, 2024

Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.
FDA Devices Moderate Feb 7, 2024

Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
FDA Devices Moderate Feb 7, 2024

Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.
FDA Devices Moderate Feb 7, 2024

Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.
FDA Devices Moderate Feb 7, 2024

SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
FDA Devices Low Jan 31, 2024

Achieva 3.0T, Model No. 781177
FDA Devices Low Jan 31, 2024

SmartPath to dStream for 1.5T, Model No. 781260, 782112
FDA Devices Low Jan 31, 2024

Intera 1.5T, Model No. 781195
FDA Devices Low Jan 31, 2024

Achieva 1.5T, Model No. 781178, 781196, 781296
FDA Devices Low Jan 31, 2024

Achieva 1.5T Conversion, Model No. 781283
FDA Devices Low Jan 31, 2024

Ingenia Ambition X, Model No. 782109
FDA Devices Moderate Jan 24, 2024

Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
FDA Devices Moderate Jan 24, 2024

(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424
FDA Devices Moderate Jan 24, 2024

(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
FDA Devices Moderate Jan 17, 2024

BrightView X, Gamma Camera, Product Code 882478

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