PlainRecalls

Philips Electronics North America Corporation

Compiled from official public sources by the publisher.

160 recalls on record · Latest: Dec 26, 2018

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Agency notice ledger

Federal filing book Philips Electronics North A… HEAVY-BOOK · SINGLE-AGENCY

#100 of 14,151 · 160 notices · 0.153% archive

  • BOOK 160 notices
  • RANK #100 of 14,151
  • SHARE 0.153% archive
  • AGENCY FDA Devices (160)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 26, 2018
  • PHOTO Stryker Instruments D…

Nearest notice-volume peer: Stryker Instruments Div. of Stryker Corporation (1 notice gap)

Philips Electronics North America Corporation accounts for about 0.153% of the 104,423-notice archive on 160 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 →

Where Philips Electronics North A… sits among 14,151 recalling firms

Philips Electronics North America Corporation ranks 100th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips Electronics North A… vs all firms by recall-notice count

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

160 100th of 14151 higher than 14,051 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 Electronics North A… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Electronics North America Corporation holds about 0.153% of archive notices alongside 160 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 23, 2015

Philips Healthcare Ingenuity Core Computed Tomography X-ray system
FDA Devices Moderate Dec 23, 2015

Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system
FDA Devices Moderate Dec 23, 2015

Philips Healthcare Ingenuity CT Computed Tomography X-ray system
FDA Devices Moderate Dec 23, 2015

Philips Healthcare Brilliance 64 Computed Tomography X-ray system
FDA Devices Moderate Dec 2, 2015

Philips HeartStart MRx Monitor/Defibrillator; M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6. For use for the termination of ventricular tachycardia and ventricular fibrillation.
FDA Devices Moderate Nov 25, 2015

ECG Out Cable,for use with a Philips ALS monitor/ defibrillator and bedside monitor for Synchronized cardioversion and Transcutaneous pacing. M1783A/M5526A 12-pin Sync cables, used with HeartStart MRx and HeartStart XL and HeartStart XL+
FDA Devices Moderate Sep 2, 2015

Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 Product Usage: The DigitalDiagnost is intended for use in generating radiographic images of human anatomy by qualified/trained doctors or technicians.
FDA Devices Moderate Aug 12, 2015

Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation. When operating as a semi-automatic external defibrillator in AED Mode, the HeartStart XL+ is suitable for use by medical personnel trained in basic life support that includes the use of an AED. When operating in Mon
FDA Devices Moderate Aug 5, 2015

Invivo Expression MRI Patient Monitoring System.
FDA Devices Moderate Jul 29, 2015

Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800220161, 459800232931, 459800235871, 459800338451. UPDATED: Pinnacle3 Software Version 8.0h, 8.0k, 8.0m, 8.0n.

Philips Electronics North A… 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 (160 here — heavy-book).

Stryker Instruments Div. of Stryker Corporation 161 Audi 162 Dr. Reddy's Laboratories, Inc. 163 Dodge 157 Synthes (USA) Products LLC 164

Frequently Asked Questions

How many federal recall notices name Philips Electronics North A…? ▼
PlainRecalls indexes 160 distinct federal recall events naming Philips Electronics North America Corporation, 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 Electronics North A… sit among other recalling firms? ▼
Philips Electronics North America Corporation ranks #100 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 Electronics North A…'s notices? ▼
FDA Devices accounts for 160 of this firm's 160 indexed notices.
What product category dominates Philips Electronics North A…'s filing book? ▼
Filings for Philips Electronics North America Corporation 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 Electronics North America Corporation: 160 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 Electronics North America Corporation; individual notices remain authoritative on each linked recall page.

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