PlainRecalls

Philips Medical Systems (Cleveland) Inc

Compiled from official public sources by the publisher.

315 recalls on record · Latest: Sep 24, 2025

Subscribe to new Philips Medical Systems recalls (RSS)

Agency notice ledger

Federal filing book Philips Medical Systems HEAVY-BOOK · SINGLE-AGENCY

#34 of 14,151 · 315 notices · 0.302% archive

  • BOOK 315 notices
  • RANK #34 of 14,151
  • SHARE 0.302% archive
  • AGENCY FDA Devices (315)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 24, 2025
  • PHOTO Whole Foods Market

Nearest notice-volume peer: Whole Foods Market (3 notice gap)

Philips Medical Systems (Cleveland) Inc accounts for about 0.302% of the 104,423-notice archive on 315 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 compares to 14,151 recalling firms

Philips Medical Systems (Cleveland) Inc ranks 34th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Philips Medical Systems vs all firms by recall-notice count

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

315 34th of 14151 higher than 14,117 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 Medical Systems in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Medical Systems (Cleveland) Inc holds about 0.302% of archive notices alongside 315 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 18, 2017

IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. The IQon Spectral CT system acquires one CT dataset composed of data from a higher-energy detected x-
FDA Devices Moderate Jan 18, 2017

FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and accessories.
FDA Devices Moderate Dec 14, 2016

Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and equipment supports, components, and accessories
FDA Devices Moderate Dec 14, 2016

Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provide information about the chemical composition of the body materials and/or contrast agents.
FDA Devices Moderate Dec 14, 2016

Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and equipment supports, components, and accessories
FDA Devices Moderate Dec 14, 2016

Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and equipment supports, components, and accessories
FDA Devices Moderate Dec 14, 2016

IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
FDA Devices Moderate Dec 14, 2016

Ingenuity Core 128 728323
FDA Devices Moderate Dec 14, 2016

Brilliance 64 728232 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and equipment supports, components, and accessories
FDA Devices Low Nov 23, 2016

Brilliance iCT Computed Tomography X-ray system, Model 728306
FDA Devices Low Nov 23, 2016

Ingenuity Core Computed Tomography X-ray system, Model 728321
FDA Devices Low Nov 23, 2016

Brilliance ICT SP Computed Tomography X-ray system, Model 728311
FDA Devices Low Nov 23, 2016

IQon Spectral CT Computed Tomography X-ray system, Model 728332
FDA Devices Low Nov 23, 2016

Ingenuity Core 128 Computed Tomography X-ray system, Model 728323
FDA Devices Low Nov 23, 2016

Ingenuity CT Computed Tomography X-ray system, Model 728326
FDA Devices Moderate Sep 14, 2016

BrightView XCT Model 882482, gamma camera for Single Photon Emission Computed Tomography (SPECT)
FDA Devices Moderate Sep 14, 2016

BrightView XCT Upgrade Model 882454
FDA Devices Moderate Sep 14, 2016

BrightView X, model #882478; gamma camera designed for single or dual detector nuclear imaging
FDA Devices Moderate Aug 31, 2016

Brilliance CT 16 Power, Model number 728240 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Brilliance CT Big Bore Oncology, Model number 728243 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Brilliance BigBore Radiology CT Model number 728244 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Brilliance 16, Model number 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Ingenuity Core, Model number 728321 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 31, 2016

Ingenuity Core128, Model number 728323 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Brilliance 64 CT Model 728231; To produce cross-sectional images of the body.
FDA Devices Moderate Aug 17, 2016

MX 16-slice SKD whole body computed tomography X-ray system. Imaging diagnostic tool.
FDA Devices Moderate Aug 17, 2016

Brilliance iCT SP Model No. 728311; To produce cross-sectional images of the body.
FDA Devices Moderate Aug 17, 2016

Brilliance 16 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Brilliance BigBore Oncology Computed Tomography X-ray systems, intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Ingenuity Core 128 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Brilliance BigBore Radiology Computed Tomography X-ray systems, intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Ingenuity Core Model No. 728321; To produce cross-sectional images of the body.
FDA Devices Moderate Aug 17, 2016

Ingenuity CT Model No. 728326; To produce cross-sectional images of the body.
FDA Devices Moderate Aug 17, 2016

Brilliance 64 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Brilliance CT 16 Power Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic tool.
FDA Devices Moderate Aug 17, 2016

Brilliance iCT, Model No. 728306; To produce cross-sectional images of the body.
FDA Devices Moderate Aug 17, 2016

Ingenuity Core Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
FDA Devices Moderate Aug 17, 2016

Ingenuity Core128 Model No. 728323; To produce cross-sectional images of the body.
FDA Devices Moderate Jul 6, 2016

Big Bore Radiology tomography X-ray system scanner, model number 728244. The Big Bore Radiology scanner is a whole body computed tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
FDA Devices Moderate Jul 6, 2016

Brilliance iCT model #728306; Intended to produce cross- sectional images of the body.
FDA Devices Moderate Jul 6, 2016

Brilliance CT Big Bore Oncology, model #728243; Intended to produce cross- sectional images of the body.
FDA Devices Moderate Jul 6, 2016

Ingenuity Core 128, model #728323; Intended to produce cross- sectional images of the body.
FDA Devices Moderate Jul 6, 2016

Brilliance 64, Computed Tomography X-ray system Product Usage: The Brilliance CT 64 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes
FDA Devices Moderate Jul 6, 2016

Big Bore Oncology tomography X-ray system scanner, model number 728243. The Big Bore Oncology scanner is a whole body computed tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes
FDA Devices Moderate Jul 6, 2016

Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The Ingenuity Core 128 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes..
FDA Devices Moderate Jul 6, 2016

Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity Core scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
FDA Devices Moderate Jul 6, 2016

Ingenuity Core, model # 728326; Intended to produce cross- sectional images of the body.
FDA Devices Moderate Jul 6, 2016

Ingenuity Flex, model # 728317; Intended to produce cross- sectional images of the body.

Philips Medical Systems 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.

Beckman Coulter, Inc. 332 Windstone Medical Packaging, Inc. 336 Smiths Medical Asd, Inc. 293 Covidien LLC 340

Frequently Asked Questions

How many federal recall notices name Philips Medical Systems? ▼
PlainRecalls indexes 315 distinct federal recall events naming Philips Medical Systems (Cleveland) Inc, 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 sit among other recalling firms? ▼
Philips Medical Systems (Cleveland) Inc ranks #34 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 Medical Systems's notices? ▼
FDA Devices accounts for 315 of this firm's 315 indexed notices.
What product category dominates Philips Medical Systems's filing book? ▼
Filings for Philips Medical Systems (Cleveland) Inc 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 (Cleveland) Inc: 315 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 (Cleveland) Inc; individual notices remain authoritative on each linked recall page.

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