PlainRecalls

Philips North America

Compiled from official public sources by the editorial team.

126 recalls on record · Latest: May 6, 2026

Philips North America Recall Insight

Philips North America appears on 126 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.124% 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 May 6, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 3 critical, 41 moderate, and 6 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Jan 17, 2024 to Aug 6, 2025.

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 Aug 6, 2025

Intera 3.0T Quasar Dual Model Number (REF): 781150;

FDA Devices Moderate Aug 6, 2025

Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;

FDA Devices Moderate Aug 6, 2025

SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;

FDA Devices Moderate Aug 6, 2025

MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;

FDA Devices Moderate Aug 6, 2025

Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva Nova-Dual Product Number: 781173;

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Explorer/Nova Dual Product Number: 781108;

FDA Devices Moderate Jun 18, 2025

SmartPath to dStream for 1.5T¿; Product Number: 782146;

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva IT Nova Product Number: 781175

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Achieva Nova Product Number: 781172;

FDA Devices Moderate Jun 18, 2025

Intera Achieva 1.5T Pulsar; Product Number: 781171;

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Master/Nova Product Number: 781106;

FDA Devices Moderate Jun 18, 2025

Intera 1.5T Omni/Stellar; Product Number: 781104;

FDA Devices Moderate Jun 18, 2025

Achieva XR Product Numbers: (1) 781153, (2) 781253;

FDA Devices Moderate Oct 16, 2024

Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1

FDA Devices Moderate Oct 9, 2024

IntelliVue G7m Anesthesia Gas Module, Product Number 866173

FDA Devices Moderate Oct 2, 2024

IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 866064), and MX…

FDA Devices Moderate Apr 17, 2024

PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional…

FDA Devices Moderate Apr 3, 2024

CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X

FDA Devices Moderate Apr 3, 2024

Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X

FDA Devices Moderate Feb 21, 2024

ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150

FDA Devices Moderate Feb 21, 2024

ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110

FDA Devices Critical Feb 14, 2024

BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4…

FDA Devices Moderate Feb 14, 2024

Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

FDA Devices Critical Feb 14, 2024

BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161

FDA Devices Moderate Feb 14, 2024

Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

FDA Devices Critical Feb 14, 2024

BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;

FDA Devices Moderate Feb 14, 2024

Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

FDA Devices Moderate Feb 7, 2024

Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.

FDA Devices Moderate Feb 7, 2024

SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129.

FDA Devices Moderate Feb 7, 2024

Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.

FDA Devices Moderate Feb 7, 2024

Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.

FDA Devices Moderate Feb 7, 2024

Achieva XR. Model (REF) Numbers 781153, 781253.

FDA Devices Moderate Feb 7, 2024

Achieva 1.5T Initial system. Model (REF) Numbers 781178.

FDA Devices Moderate Feb 7, 2024

Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.

FDA Devices Moderate Feb 7, 2024

Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.

FDA Devices Moderate Feb 7, 2024

Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.

FDA Devices Moderate Feb 7, 2024

Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.

FDA Devices Moderate Feb 7, 2024

Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.

FDA Devices Moderate Feb 7, 2024

SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.

FDA Devices Low Jan 31, 2024

Achieva 3.0T, Model No. 781177

FDA Devices Low Jan 31, 2024

SmartPath to dStream for 1.5T, Model No. 781260, 782112

FDA Devices Low Jan 31, 2024

Intera 1.5T, Model No. 781195

FDA Devices Low Jan 31, 2024

Achieva 1.5T, Model No. 781178, 781196, 781296

FDA Devices Low Jan 31, 2024

Achieva 1.5T Conversion, Model No. 781283

FDA Devices Low Jan 31, 2024

Ingenia Ambition X, Model No. 782109

FDA Devices Moderate Jan 24, 2024

Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871

FDA Devices Moderate Jan 24, 2024

(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424

FDA Devices Moderate Jan 24, 2024

(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436

FDA Devices Moderate Jan 17, 2024

BrightView X, Gamma Camera, Product Code 882478

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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.