Philips North America
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.
Intera 3.0T Quasar Dual Model Number (REF): 781150;
Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
Intera 1.5T Achieva Nova-Dual Product Number: 781173;
Intera 1.5T Explorer/Nova Dual Product Number: 781108;
SmartPath to dStream for 1.5T¿; Product Number: 782146;
Intera 1.5T Achieva IT Nova Product Number: 781175
Intera 1.5T Achieva Nova Product Number: 781172;
Intera Achieva 1.5T Pulsar; Product Number: 781171;
Intera 1.5T Master/Nova Product Number: 781106;
Intera 1.5T Omni/Stellar; Product Number: 781104;
Achieva XR Product Numbers: (1) 781153, (2) 781253;
Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 866064), and MX…
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…
CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4…
Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161
Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;
Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129.
Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
Achieva XR. Model (REF) Numbers 781153, 781253.
Achieva 1.5T Initial system. Model (REF) Numbers 781178.
Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.
Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.
Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.
SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
Achieva 3.0T, Model No. 781177
SmartPath to dStream for 1.5T, Model No. 781260, 782112
Intera 1.5T, Model No. 781195
Achieva 1.5T, Model No. 781178, 781196, 781296
Achieva 1.5T Conversion, Model No. 781283
Ingenia Ambition X, Model No. 782109
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
(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
BrightView X, Gamma Camera, Product Code 882478
Nearby Manufacturers
Other firms with recall activity tracked in the PlainRecalls index.
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.