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 Feb 27, 2019

PageWriter TC50 Government Bundle, Product 860429, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
FDA Devices Moderate Dec 19, 2018

HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx Monitor/Defibrillators.
FDA Devices Critical Feb 14, 2018

MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician
FDA Devices Critical Apr 5, 2017

HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9

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