PlainRecalls

Philips North America

73 recalls on record · Latest: Feb 4, 2026

Philips North America Recall Insight

Philips North America appears on 73 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.087% 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 4, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 23 entries, severity tagging shows 0 critical, 21 moderate, and 2 lower-severity recalls. Affected-unit counts are disclosed on 19 of 23 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 (23). The date window on this page runs from May 24, 2023 to Jan 31, 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 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 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 17, 2024

BrightView X, Gamma Camera, Product Code 882478

FDA Devices Moderate Jan 17, 2024

(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)

FDA Devices Moderate Jan 17, 2024

BrightView, Gamma Camera System, Product Code 882480.

FDA Devices Moderate Jan 17, 2024

BrightView XCT, Gamma Camera, Product Code 882482

FDA Devices Moderate Nov 22, 2023

Spectral CT on Rails, Software Version 5.1.0, Model Number 728334

FDA Devices Moderate Nov 22, 2023

Spectral CT on Rails, Software Version 5.1.0, Model Number 728334

FDA Devices Moderate Nov 15, 2023

Allura Xper IGTS Fixed Systems

FDA Devices Moderate Nov 15, 2023

BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery C-arm systems.

FDA Devices Moderate Nov 15, 2023

Veradius Unity Mobile Surgery C-arm

FDA Devices Moderate Nov 15, 2023

Zenition 50 & 70 Mobile Surgery C-arm

FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)

FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)

FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)

FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)

FDA Devices Moderate Aug 9, 2023

Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146

FDA Devices Moderate May 24, 2023

ProxiDiagnost N90 R.1.0

FDA Devices Moderate May 24, 2023

CombiDiagnost R90 R.1.0

FDA Devices Moderate May 24, 2023

CombiDiagnost R90 R1.1

FDA Devices Moderate May 24, 2023

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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