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 Mar 6, 2019

Intera Achieva 1.5T IT Nova Dual, Model Number 781176. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T TX-series, Model Number 781278. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Prodiva CX, Model Number 781070. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva XR 1.5T/3.0T , Model Number 781253. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera Achieva 1.5T IT Nova, Model Number 781175. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T, Model Number 781178. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia Ambition X, Model Number 781356. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia Elition S, Model Number 781357. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T, Model Number 781177. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Ingenia Ambition S, Model Number 781359. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

MR-OR 1.5T, Model Number 781437. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Panorama 1.0T, Model Number 781250. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 0.5T Standard, Model Number 781101. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Achieva 1.5T, Model Number 781343. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Mar 6, 2019

Intera 1.5T High Performance, Model Number 781295. Nuclear Magnetic Resonance Imaging System
FDA Devices Moderate Jan 16, 2019

Ingenia Elition S, Ingenia Elition X
FDA Devices Moderate Jul 4, 2018

OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
FDA Devices Moderate Jul 4, 2018

OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
FDA Devices Moderate May 9, 2018

Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

MultiDiagnost Eleva 708036 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
FDA Devices Moderate May 9, 2018

MultiDim Eleva 708032 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.

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