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Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips Recalls

All product recalls associated with Philips Medical Systems North America Co. Phillips.

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Recall Summary

Total Recalls

1000

Past Year

631

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 9601–9620 of 10391 recalls

Philips Medical Systems North America Co. Phillips: Allura Xper FD20 X-Ray System, Release 2.2, Philips Medic...

Inaccurate anatomical measurements when using the optional SmartMask feature

FDASep 24, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Nicolet Biomedical Div of Viasys Healthcare: Viasys Healthcare NicoletOne ICU Monitor, Modular Neurod...

Display lock-up: VIASYS Healthcare NicoletOne ICU Monitor freezes up during operation when using the digital video option.

FDASep 11, 2007Nationwide• Nicolet Biomedical Div of Viasys Healthcare

GE Healthcare: GE Healthcare Advantage Workstations, Advantage Worksatio...

Aortic Length over-estimated: incorrect measurements when using the Aorta analysis protocol or customized protocols. Until a new software version is installed the aorta analysis protocol or the customized protocols for an aneurysm should NOT BE USED.

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FDASep 10, 2007AL, AK, AZ +46 more• GE Healthcare

OrthoHelix Surgical Designs Inc: DRL System Trays comprised of DRLock Bone Fixation Plate...

Seat/Fit problems: The heads of the distal screws/pegs rest above the surface of the distal plate after the screws/pegs are fully tightened.

FDASep 4, 2007Nationwide• OrthoHelix Surgical Designs Inc

GE Healthcare Clinical Systems: GE LOGIQ 3 Expert ultrasound scanner with software versio...

Inaccurate guidelines: The BE9C is an optional, small radius Bi-planar convex probe intended for use with the LOGIQ 3 Expert system in Urology application. An attempt by the user to activate the biopsy guidelines while this probe is in use will cause incorrect guidelines to be displayed on the image. The incorrect guidelines are recognized by their orientation that is left/right reversed from t

FDASep 4, 2007AL, NY• GE Healthcare Clinical Systems

Cardinal Health 303 Inc DBA Alaris Products: Texium Closed Male Luer (CML), Model Number 10012241, Ca...

Leaks: there is a risk of leakage at the female end of the Texium closed male luer (CML) when attached to a spin luer. (NOTE: users who connect the female portion of the Texium closed male luer to fixed (one-piece) male luers on tubing or on syringes are not affected by this issue)

FDAAug 30, 2007AR, CA, CO +22 more• Cardinal Health 303 Inc DBA Alaris Products

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 7...

An issue with the Paceart System - 2006 First Edition (Get Connected Edition) exists. Under certain circumstances, Paceart System Generic ICD reports may not accurately reflect patient VT/VF, SVT/NST and Mode Switch/AT/AF episode detection data. When episode detection data is imported into the Paceart System from certain sources, the Paceart System Generic ICD reports display a zero, suggesting

FDAAug 27, 2007Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Backpack Blowers (Shindaiwa) – Fire Risk (2007)

Fire/Burn Risk

This recall involves Shindaiwa Models EB8510 and EB8510RT. All models up to serial #7025018 are included. After serial number 7025018, the leaf blower has been upgraded with stainless steel muffler shells. The backpack blowers weight approximately 24 pounds and include Serial Numbers through February 2007 production (S/N 702XXXX) which are located on the side label. These machines are blue, with a red label that reads "Shindaiwa".

CPSCAug 24, 2007Nationwide• Shindaiwa Kogyo Co., Ltd., Hiroshima, Japan

Philips Medical Systems North America Co. Phillips: Philips Medical System - BV Pulsera Mobile C-arms with Re...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Medical System - Endura X-Ray Systems (Release 2)...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew, CALAXO Bioabsorbable lnterference Screw, ...

Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation.

FDAAug 21, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Baxter Healthcare Corp. Rt.: Baxter Colleague CX Single Channel Volumetric Infusion Pu...

Some of the pumps were upgraded by one service technician who failed to replace prisms and batteries as required in the upgrade.

FDAAug 15, 2007CA, FL• Baxter Healthcare Corp. Rt.

Cardinal Health 303 Inc DBA Alaris Products: Pyxis Anesthesia System 3500, Cardinal Health, Clinical T...

System lock up; mini-drawers -under certain circumstances during use, are not accessable, delaying the user from accessing critical medications.

FDAAug 13, 2007Nationwide• Cardinal Health 303 Inc DBA Alaris Products

GE Healthcare: GE Definium 8000 , model 5135678, Digital Radiographic Sy...

Necessary certification labels are missing from the x-ray contol.

FDAAug 13, 2007Nationwide• GE Healthcare

GE Healthcare: GE Precision 500D, model 2403790-3, Radiographic and Fluo...

Necessary certification labels are missing from the x-ray contol.

FDAAug 13, 2007Nationwide• GE Healthcare

Garden Treasures Cloud 9 Chair (Taizhou Yongjiang) – fall hazard (2007)

This recall involves the Garden Treasures Cloud 9 Beyond outdoor lounge chairs. The chairs are tan in color, have a light steel frame, cloth seat, a pillow at the headrest and an adjustable sun visor.

CPSCAug 9, 2007Nationwide• Taizhou Yongjiang Arts and Crafts Collective Ltd., of China

E Light (Plan 9) – fire hazard (2007)

Fire/Burn Risk

The E Light is a 12-Volt DC light fixture with recessed LEDs typically mounted on the ceiling or under a counter. The recalled light is a flat, white rectangle with three LEDs (in the three-watt model) or six LEDs (in the six-watt model).

CPSCAug 3, 2007Nationwide• Plan 9 Inc., of White Salmon, Wash.

Raleigh Cadent Bicycle (Carbonage) – fork break risk (2007)

The recall involves the 2007 Raleigh Cadent 1.0, Cadent 2.0 and Cadent Carbon bicycle models with carbon forks. "Raleigh" is printed on the down tube of the bicycle, and the model name is printed on the top tube.

CPSCAug 3, 2007Nationwide• Carbonage Technology, of Baoan, China

Hi-Heat Aerosol Coating (Sherwin-Williams) – explosion risk (2007)

The recall involves Thermo-Tec Hi-Heat aerosol coating used to color and protect Thermo-Tec automotive exhaust wrap. The part number (#12002) is printed above the UPC, and the date code (#B1815) is written on the bottom of the can. The 11-ounce aerosol can is mostly blue with orange and yellow flames and has an aluminum-colored cap. The can states "HI-HEAT COATING 2000°F" in large white letters on the front of the can.

CPSCAug 3, 2007Nationwide• The Sherwin-Williams Co., of Cleveland, Ohio

GE Healthcare: Sunisa Flexi-DT Table, Model Numbers: 51335678, 2269647, ...

Fire/Burn Risk

Design Problems Including: 1) Hot Brake (Longitudinal Overheating) potential risk of burns 2) Brake Locks and Sudden Releases 3) Emergency Stop Circuit Button; open instead of closed 4) Longitudinal Brakes Release does not engage properly 5) Tilting Movement causing tabletop to slide; may cause risk of pinched fingers to patient and/or operator 6) Lodging Pins on floor Uncovered; may cause potenti

FDAAug 1, 2007AL, CA, FL +11 more• GE Healthcare