PlainRecalls

Philips Medical Systems Gmbh, Dmc

33 recalls on record · Latest: Sep 8, 2021

Philips Medical Systems Gmbh, Dmc Recall Insight

Philips Medical Systems Gmbh, Dmc appears on 33 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.032% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Sep 8, 2021, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 33 entries, severity tagging shows 0 critical, 33 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 7 of 33 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (33). The date window on this page runs from Aug 29, 2018 to Sep 8, 2021.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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, 71…

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

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.