PlainRecalls

Philips Medical Systems Gmbh, Dmc

Compiled from official public sources by the publisher.

33 recalls on record · Latest: Sep 8, 2021

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Agency notice ledger

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

#513 of 14,151 · 33 notices · 0.032% archive

  • BOOK 33 notices
  • RANK #513 of 14,151
  • SHARE 0.032% archive
  • AGENCY FDA Devices (33)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 8, 2021
  • PHOTO Avkare Inc.

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

Philips Medical Systems Gmbh, Dmc accounts for about 0.032% of the 104,423-notice archive on 33 distinct filings — a mid 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 Gmb… compares to 14,151 recalling firms

Philips Medical Systems Gmbh, Dmc ranks 513th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

33 513th of 14151 higher than 13,632 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 Gmb… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Philips Medical Systems Gmbh, Dmc holds about 0.032% of archive notices alongside 33 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 8, 2021

CombiDiagnost R90 Software Version R1.0 and R1.1
FDA Devices Moderate Feb 26, 2020

CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
FDA Devices Moderate Feb 26, 2020

CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
FDA Devices Moderate Feb 20, 2019

Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
FDA Devices Moderate Oct 31, 2018

Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.
FDA Devices Moderate Aug 29, 2018

BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Single Detector (Stitching Patient Support) 712020
FDA Devices Moderate Aug 29, 2018

EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Release 3 (Stitching Patient Support) 712025
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Release 3 (Stitching Patient Support) 712025
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Upgrades (Stitching Patient Support) 712083
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
FDA Devices Moderate Aug 29, 2018

EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 (Stitching Patient Support) 712225
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
FDA Devices Moderate Aug 29, 2018

CombiDiagnost R90 (Stitching Patient Support) 709030
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084

Philips Medical Systems Gmb… holds a measurable archive slice

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.

CooperVision, Inc. 33 Custom Healthcare Systems, Inc. 33 Implant Direct Sybron Manufacturing LLC 33 Medtronic MiniMed 33

Frequently Asked Questions

How many federal recall notices name Philips Medical Systems Gmb…? ▼
PlainRecalls indexes 33 distinct federal recall events naming Philips Medical Systems Gmbh, Dmc, 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 Gmb… sit among other recalling firms? ▼
Philips Medical Systems Gmbh, Dmc ranks #513 of 14,151 by distinct recall-event count among 14,151 firms in this archive (96th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips Medical Systems Gmb…'s notices? ▼
FDA Devices accounts for 33 of this firm's 33 indexed notices.
What product category dominates Philips Medical Systems Gmb…'s filing book? ▼
Filings for Philips Medical Systems Gmbh, Dmc 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 Gmbh, Dmc: 33 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 Gmbh, Dmc; individual notices remain authoritative on each linked recall page.

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