PlainRecalls

Philips North America Llc

Compiled from official public sources by the publisher.

404 recalls on record · Latest: Jul 1, 2026

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Agency notice ledger

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

#23 of 14,151 · 404 notices · 0.387% archive

  • BOOK 404 notices
  • RANK #23 of 14,151
  • SHARE 0.387% archive
  • AGENCY FDA Devices (404)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 1, 2026
  • PHOTO Bmw

Nearest notice-volume peer: Bmw (4 notice gap)

Philips North America Llc accounts for about 0.387% of the 104,423-notice archive on 404 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 Llc compares to 14,151 recalling firms

Philips North America Llc ranks 23rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips North America Llc vs all firms by recall-notice count

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

404 23rd of 14151 higher than 14,128 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 North America Llc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips North America Llc holds about 0.387% of archive notices alongside 404 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 8, 2024

The Oncology Essentials Package of the Spectral CT imaging system.
FDA Devices Moderate May 1, 2024

Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterruptable Power Supply Model: SCL500RM1U 2. APC (Schneider Electric IT Corporation) 230V Uninterruptable Power Supply Model: SCL500RMI1U
FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T S, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 1.5T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Omni/Stellar, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 3.0T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

GYROSCAN T5-NT, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva IT Nova, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.0T Omni/Stellar, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

GYROSCAN ACS-NT, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva XR, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T CX, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia Elition S, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia Elition X, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Enterprise 1.5T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

MR 7700, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

GYROSCAN T5, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 3.0TX for PET, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera CV, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 1.5T Conversion, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T R11, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 1.5T Initial, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.0T Power/Pulsar, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Evolution Upgrade 3.0T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

SmartPath to dStream for 1.5T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Achieva 3.0T for PET, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

MR 5300, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia Ambition X, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Power/Pulsar, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 0.5T Standard, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

GYROSCAN T10-NT, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 3.0T Quasar Dual, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia 3.0T, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia Ambition S, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Intera 1.5T Master/Nova, Magnetic Resonance System.
FDA Devices Moderate Apr 24, 2024

Ingenia 3.0T CX, Magnetic Resonance System.
FDA Devices Moderate Jan 24, 2024

Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
FDA Devices Moderate Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body taken at different angles and planes. The system also includes signal analysis and display equipment, patient and equipment supports, components, and accessories. Philips Inclusive CT has a 72cm bore and includes a detector array that provides 50cm scan field of view.
FDA Devices Critical Dec 20, 2023

Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Systems for use as a diagnostic device.
FDA Devices Moderate Nov 29, 2023

SmartPath to dStream for 1.5T
FDA Devices Moderate Nov 29, 2023

Ingenia 1.5T CX
FDA Devices Moderate Nov 29, 2023

Achieva 1.5T
FDA Devices Moderate Nov 29, 2023

Achieva 1.5T Initial System

Philips North America Llc carries an outsized archive share

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.

Baxter Healthcare Corporation 413 Olympus Corporation of the Americas 414 Biomerieux Inc 422 B Braun Medical Inc 444

Frequently Asked Questions

How many federal recall notices name Philips North America Llc? ▼
PlainRecalls indexes 404 distinct federal recall events naming Philips North America Llc, 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 Llc sit among other recalling firms? ▼
Philips North America Llc ranks #23 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 Llc's notices? ▼
FDA Devices accounts for 404 of this firm's 404 indexed notices.
What product category dominates Philips North America Llc's filing book? ▼
Filings for Philips North America Llc 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 Llc: 404 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 Llc; individual notices remain authoritative on each linked recall page.

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