PlainRecalls

Philips Healthcare

Compiled from official public sources by the publisher.

21 recalls on record · Latest: Oct 11, 2023

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Agency notice ledger

Federal filing book Philips Healthcare MID-BOOK · SINGLE-AGENCY

#782 of 14,151 · 21 notices · 0.020% archive

  • BOOK 21 notices
  • RANK #782 of 14,151
  • SHARE 0.020% archive
  • AGENCY FDA Devices (21)
  • CAT medical devices
  • CATS 1 category
  • LATEST Oct 11, 2023
  • PHOTO A&h Focal Inc.

Nearest notice-volume peer: A&h Focal Inc. (0 notice gap)

Philips Healthcare accounts for about 0.020% of the 104,423-notice archive on 21 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 →

Philips Healthcare's standing among 14,151 recalling firms

Philips Healthcare ranks 782nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips Healthcare vs all firms by recall-notice count

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

21 782nd of 14151 higher than 13,362 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 Healthcare in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Healthcare holds about 0.020% of archive notices alongside 21 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Oct 11, 2023

Incisive CT, software version 5.0
FDA Devices Moderate Apr 13, 2022

Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x
FDA Devices Moderate Mar 30, 2022

Azurion systems with software release R2.0.x
FDA Devices Moderate Dec 1, 2021

CombiDiagnost R90 is multi-functional general R/F systems.
FDA Devices Moderate Dec 1, 2021

DigitalDiagnost C90
FDA Devices Moderate Dec 1, 2021

Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)
FDA Devices Moderate Dec 1, 2021

ProxiDiagnost N90 is multi-functional general R/F systems.
FDA Devices Moderate Oct 2, 2019

DigitalDiagnost C50, Stationary X-ray System
FDA Devices Moderate Aug 1, 2018

Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA,stent placing,atherectomies), pacemaker implantat ions, and electrophysiology (EP). Non-vascular interventions such as drainages,biopsies and vertebroplasties procedures.
FDA Devices Moderate Aug 1, 2018

UNIQ Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA,stent placing,atherectomies), pacemaker implantat ions, and electrophysiology (EP). Non-vascular interventions such as drainages,biopsies and vertebroplasties procedures.
FDA Devices Moderate Aug 1, 2018

Allura Xper Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA,stent placing,atherectomies), pacemaker implantat ions, and electrophysiology (EP). Non-vascular interventions such as drainages,biopsies and vertebroplasties procedures.
FDA Devices Moderate Jun 15, 2016

Philips Healthcare DigitalDiagnost stationary X-ray system
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare DuraDiagnost stationary X-ray system
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance 64 Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Core Computed Tomography X-Ray System
FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity CT Computed Tomography X-Ray System
FDA Devices Moderate Feb 5, 2014

InnerCool RTx Endovascular System, Model Numbers: 861470 (120V), 861472 (240V). Product Usage: The InnerCool RTx device is a thermal regulating system intended to induce, maintain and reverse mild hypothermia, to achieve and/or maintain normothermia, and for use in fever reduction. K080908

Philips Healthcare holds a measurable archive slice

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 (21 here).

A&h Focal Inc. 21 Able Groupe Inc 21 Alvogen, Inc 21 Aroa Biosurgery, LTD. 21 Aston Martin 21

Similar medical devices volume

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

Aroa Biosurgery, LTD. 21 Corin Ltd 21 Covidien 21 Custom Medical Specialties, Inc. 21

Frequently Asked Questions

How many federal recall notices name Philips Healthcare? ▼
PlainRecalls indexes 21 distinct federal recall events naming Philips Healthcare, 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 Healthcare sit among other recalling firms? ▼
Philips Healthcare ranks #782 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips Healthcare's notices? ▼
FDA Devices accounts for 21 of this firm's 21 indexed notices.
What product category dominates Philips Healthcare's filing book? ▼
Filings for Philips Healthcare 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 Healthcare: 21 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 Healthcare; individual notices remain authoritative on each linked recall page.

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