Philips North America, LLC
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.
Intera 1.5T Omni/Stellar, Magnetic Resonance System.
Achieva 3.0T, Magnetic Resonance System.
GYROSCAN T5-NT, Magnetic Resonance System.
Intera 1.5T, Magnetic Resonance System.
Intera 1.5T Achieva Nova, Magnetic Resonance System.
Intera 1.5T Achieva IT Nova, Magnetic Resonance System.
Intera 1.0T Omni/Stellar, Magnetic Resonance System.
GYROSCAN ACS-NT, Magnetic Resonance System.
Achieva XR, Magnetic Resonance System.
Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
Ingenia 1.5T CX, Magnetic Resonance System.
Ingenia Elition S, Magnetic Resonance System.
Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
Ingenia Elition X, Magnetic Resonance System.
Enterprise 1.5T, Magnetic Resonance System.
MR 7700, Magnetic Resonance System.
GYROSCAN T5, Magnetic Resonance System.
Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
Achieva 3.0TX for PET, Magnetic Resonance System.
Intera CV, Magnetic Resonance System.
Achieva 1.5T Conversion, Magnetic Resonance System.
Intera 1.5T R11, Magnetic Resonance System.
Achieva 1.5T Initial, Magnetic Resonance System.
Intera 1.0T Power/Pulsar, Magnetic Resonance System.
Evolution Upgrade 3.0T, Magnetic Resonance System.
SmartPath to dStream for 1.5T, Magnetic Resonance System.
Achieva 3.0T for PET, Magnetic Resonance System.
MR 5300, Magnetic Resonance System.
Ingenia Ambition X, Magnetic Resonance System.
Intera 1.5T Power/Pulsar, Magnetic Resonance System.
Intera 0.5T Standard, Magnetic Resonance System.
SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
Ingenia 1.5T, Magnetic Resonance System.
GYROSCAN T10-NT, Magnetic Resonance System.
Intera 3.0T Quasar Dual, Magnetic Resonance System.
Ingenia 3.0T, Magnetic Resonance System.
Ingenia Ambition S, Magnetic Resonance System.
Intera 1.5T Master/Nova, Magnetic Resonance System.
Ingenia 3.0T CX, Magnetic Resonance System.
Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
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…
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Sy…
SmartPath to dStream for 1.5T
Ingenia 1.5T CX
Achieva 1.5T
Achieva 1.5T Initial System
Achieva 1.5T Conversion
Intera 1.5T Power/Pulsar
Intera 1.5T
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
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.