PlainRecalls

Philips Medical Systems Nederlands

Compiled from official public sources by the publisher.

79 recalls on record · Latest: Jun 30, 2021

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Agency notice ledger

Federal filing book Philips Medical Systems Ned… MID-BOOK · SINGLE-AGENCY

#228 of 14,151 · 79 notices · 0.076% archive

  • BOOK 79 notices
  • RANK #228 of 14,151
  • SHARE 0.076% archive
  • AGENCY FDA Devices (79)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 30, 2021
  • PHOTO Abiomed, Inc.

Nearest notice-volume peer: Abiomed, Inc. (0 notice gap)

Philips Medical Systems Nederlands accounts for about 0.076% of the 104,423-notice archive on 79 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 Medical Systems Ned… compares to 14,151 recalling firms

Philips Medical Systems Nederlands ranks 228th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips Medical Systems Ned… vs all firms by recall-notice count

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

79 228th of 14151 higher than 13,921 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 · 2026-09-15

Philips Medical Systems Ned… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Medical Systems Nederlands holds about 0.076% of archive notices alongside 79 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 30, 2021

Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029, 722035, 722038, and 722058.
FDA Devices Moderate Aug 7, 2019

Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
FDA Devices Moderate May 8, 2019

Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device
FDA Devices Moderate Apr 24, 2019

Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The Allura Xper FD Series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures.
FDA Devices Moderate Apr 24, 2019

Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura Xper FD10 722005 Allura Xper FD10/10 722006 Allura Xper FD20 722008 Allura Xper FD20 Biplane 722010 Allura Xper FD10 722011 Allura Xper FD10/10 722012 Allura Xper FD20 722013 Allura XPER FD20 BIPLANE 722014 Allura Xper FD10 OR Table 722015 Allura Xper FD20 OR Table 722019 Allura Xper FD10/10 OR Table 722020 Allura Xper FD20 Biplane OR Table 722022 Allura Xper FD10 O
FDA Devices Moderate Mar 6, 2019

Achieva XR 1.5T/3.0T, Model Number 781153. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

SmartPath to dStream for XR and 3.0T, Model Number 781270. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T Achieva CV Nova, Model Number 781174. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Enterprise 1.5T, Model Number 781145. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

SmartPath to dStream for 1.5T, Model Number 781260. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 3.0T, Model Number 781342. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T, Model Number 781296. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera Achieva 1.5T Nova, Model Number 781172. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T Conversion, Model Number 781283. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T Explorer/Nova Dual, Model Number 781108. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Multiva 1.5T 8 R5 (ZBO), Model Number 781072. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera Achieva 1.5T Nova Dual, Model Number 781173. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T TX, Model Number 781345. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Multiva 1.5T 8 R5, Model Number 781074. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T, Model Number 781195. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera Achieva 1.5T Pulsar, Model Number 781171. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 1.5T CX (ZBO), Model Number 781262. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T R11, Model Number 781170. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T X-series, Model Number 781277. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T Omni/Stellar, Model Number 781104. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

MARLIN 1.5T, Model Number 781474. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

NZM101 Ingenia 1.5T Linac, Model Number 781483. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T X, Model Number 781344. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T CV, Model Number 781107. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Multiva 1.5T, Model Number 781076. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T High Performance, Model Number 781196. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 3.0T Master/Quasar Dual, Model Number 781150. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 1.5T, Model Number 781341. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T TX for PET, Model Number 781479. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Panorama 1.0T, Model Number 781350. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T Master/Nova, Model Number 781106. Nuclear Magnetic Resonance Imaging System

Philips Medical Systems Ned… 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 (79 here — heavy-book).

Abiomed, Inc. 79 Key Pharmacy and Compounding Center 79 Lyons Magnus, Inc 79 Suzuki 79 Ice Cream House 80

Frequently Asked Questions

How many federal recall notices name Philips Medical Systems Ned…? ▼
PlainRecalls indexes 79 distinct federal recall events naming Philips Medical Systems Nederlands, 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 Medical Systems Ned… sit among other recalling firms? ▼
Philips Medical Systems Nederlands ranks #228 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips Medical Systems Ned…'s notices? ▼
FDA Devices accounts for 79 of this firm's 79 indexed notices.
What product category dominates Philips Medical Systems Ned…'s filing book? ▼
Filings for Philips Medical Systems Nederlands 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 Medical Systems Nederlands: 79 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 Medical Systems Nederlands; individual notices remain authoritative on each linked recall page.

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