PlainRecalls

Philips Healthcare

Compiled from official public sources by the editorial team.

21 recalls on record · Latest: Oct 11, 2023

Philips Healthcare Recall Insight

Philips Healthcare appears on 21 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.021% 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 Oct 11, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 21 entries, severity tagging shows 0 critical, 21 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 21 of 21 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 (21). The date window on this page runs from Feb 5, 2014 to Oct 11, 2023.

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 Oct 11, 2023

Incisive CT, software version 5.0

FDA Devices Moderate Apr 13, 2022

Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x

FDA Devices Moderate Mar 30, 2022

Azurion systems with software release R2.0.x

FDA Devices Moderate Dec 1, 2021

CombiDiagnost R90 is multi-functional general R/F systems.

FDA Devices Moderate Dec 1, 2021

DigitalDiagnost C90

FDA Devices Moderate Dec 1, 2021

Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)

FDA Devices Moderate Dec 1, 2021

ProxiDiagnost N90 is multi-functional general R/F systems.

FDA Devices Moderate Oct 2, 2019

DigitalDiagnost C50, Stationary X-ray System

FDA Devices Moderate Aug 1, 2018

Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasi…

FDA Devices Moderate Aug 1, 2018

UNIQ Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive …

FDA Devices Moderate Aug 1, 2018

Allura Xper Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally in…

FDA Devices Moderate Jun 15, 2016

Philips Healthcare DigitalDiagnost stationary X-ray system

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare DuraDiagnost stationary X-ray system

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance 64 Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Core Computed Tomography X-Ray System

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity CT Computed Tomography X-Ray System

FDA Devices Moderate Feb 5, 2014

InnerCool RTx Endovascular System, Model Numbers: 861470 (120V), 861472 (240V). Product Usage: The InnerCool RTx device is a thermal regulating s…

Nearby Manufacturers

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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.