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.
SmartPath to dStream for 1.5T, Model No. 781260, 782112
Intera 1.5T, Model No. 781195
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424
BrightView X, Gamma Camera, Product Code 882478
(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)
BrightView, Gamma Camera System, Product Code 882480.
BrightView XCT, Gamma Camera, Product Code 882482
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Allura Xper IGTS Fixed Systems
BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery C-arm systems.
Veradius Unity Mobile Surgery C-arm
Zenition 50 & 70 Mobile Surgery C-arm
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
ProxiDiagnost N90 R.1.0
CombiDiagnost R90 R.1.0
CombiDiagnost R90 R1.1
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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