PlainRecalls

Philips North America, LLC

Compiled from official public sources by the editorial team.

400 recalls on record · Latest: Feb 18, 2026

Philips North America, LLC Recall Insight

Philips North America, LLC appears on 400 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.393% 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 Feb 18, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 1 critical, 49 moderate, and 0 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 Nov 22, 2023 to Apr 24, 2024.

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 Apr 24, 2024

Intera 1.5T Omni/Stellar, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva 3.0T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

GYROSCAN T5-NT, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva IT Nova, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.0T Omni/Stellar, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

GYROSCAN ACS-NT, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva XR, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T CX, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia Elition S, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia Elition X, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Enterprise 1.5T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

MR 7700, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

GYROSCAN T5, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera Achieva 1.5T Pulsar, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva 3.0TX for PET, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera CV, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva 1.5T Conversion, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T R11, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva 1.5T Initial, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.0T Power/Pulsar, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Evolution Upgrade 3.0T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

SmartPath to dStream for 1.5T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Achieva 3.0T for PET, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

MR 5300, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia Ambition X, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Power/Pulsar, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 0.5T Standard, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

GYROSCAN T10-NT, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 3.0T Quasar Dual, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia 3.0T, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia Ambition S, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Master/Nova, Magnetic Resonance System.

FDA Devices Moderate Apr 24, 2024

Ingenia 3.0T CX, Magnetic Resonance System.

FDA Devices Moderate Jan 24, 2024

Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.

FDA Devices Moderate Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body…

FDA Devices Critical Dec 20, 2023

Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Sy…

FDA Devices Moderate Nov 29, 2023

SmartPath to dStream for 1.5T

FDA Devices Moderate Nov 29, 2023

Ingenia 1.5T CX

FDA Devices Moderate Nov 29, 2023

Achieva 1.5T

FDA Devices Moderate Nov 29, 2023

Achieva 1.5T Initial System

FDA Devices Moderate Nov 29, 2023

Achieva 1.5T Conversion

FDA Devices Moderate Nov 29, 2023

Intera 1.5T Power/Pulsar

FDA Devices Moderate Nov 29, 2023

Intera 1.5T

FDA Devices Moderate Nov 22, 2023

Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT scanner and simulator designed for radiation oncology and therapy.

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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.