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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

1000

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 19141–19160 of 21319 recalls

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Drew Scientific Group PLC: Bayer Advia 70 Hematology Analyzer, manufactured by Drew ...

Flags and alerts on the user interface will not automatically transfering to the LIS.

FDAAug 24, 2006FL, MA, MN +5 more• Drew Scientific Group PLC

Drew Scientific Group PLC: Drew Excell 22 Hematology Analyzer, manufactured by Drew ...

Flags and alerts on the user interface will not automatically transfering to the LIS.

FDAAug 24, 2006FL, MA, MN +5 more

1...956 957958959 960...1066

Page 958 of 1066Next

• Drew Scientific Group PLC

Lithium-Ion Batteries (Sony) – fire hazard (2006)

Fire/Burn Risk

The recalled lithium-ion batteries were used with the following computers: 12-inch iBook G4, 12-inch PowerBook G4 and 15-inch PowerBook G4. Consumers should remove the battery from the computer to view the model and serial numbers labeled on the bottom of the unit. Computer model name Battery model number Battery serial numbers 12-inch iBook G4 A1061 ZZ338 through ZZ4273K429 through 3K6116C519 through 6C552 12-inch PowerBook G4 A1079 ZZ411 through ZZ4273K428 through 3K611 15-inch PowerBook G4 A1078 and A1148 3K425 through 3K6016N530 through 6N5516N601 No other Apple notebook computers are involved in this recall.

CPSCAug 24, 2006Nationwide• Sony Energy Devices Corp., of Japan

Sunrise Medical: DeVilbiss iFill Personal Oxygen Station model number 535D.

Potential for oxygen cylinders to not fill completely

FDAAug 24, 2006Nationwide• Sunrise Medical

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10/10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Nihon Kohden America Inc: Nihon Kohden Electric Stimulator, Model number: MS-210BK ...

Fire/Burn Risk

When the device is subject to physical shock, such as a drop to the floor, it may output a different value from the preset value. This may result in a superficial burn on the patient if the stimulation is done for a long time.

FDAAug 23, 2006Nationwide• Nihon Kohden America Inc

EMD Chemicals Inc: Anaerotest;Microbiology , 50 test strips 1.15112 Store dr...

Lot # OC553145 of Anaerotest failed to remain in specification. QC indicator shows an anaerobic environment even if oxygen is present

FDAAug 17, 2006Nationwide• EMD Chemicals Inc

EMD Chemicals Inc: Anaerotest for microbiology Specification: Performance Te...

Lot # OC553145 of Anaerotest failed to remain in specification. QC indicator shows an anaerobic environment even if oxygen is present.

FDAAug 17, 2006Nationwide• EMD Chemicals Inc

Becton Dickinson & Co.: BD BBL Staphyloslide Latex Test Kit, Catalog # 240952 (1...

False Negative Staphylococcus aureus results which could prevent infected patients from receiving antimicrobial treatment; due to the failure of the Positive Control to react within 20 seconds. The failure is due to reduced reactivity of the latex component.

FDAAug 17, 2006Nationwide• Becton Dickinson & Co.

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Sys...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE O...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: RUS Tool Version Software

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Tu-Wire Dimming Ballasts (Lutron) – shock risk (2006)

The recalled ballast is used to dim compact fluorescent lighting fixtures. The ballasts are not visible once installed. The ballasts were included with light fixtures sold under numerous brand names. Consumers should not touch these fixtures, since they could pose a shock hazard. The fixtures with these ballasts have a 120 VAC application, the fixture housing is for a 26W or 32W four-pin plug-in compact fluorescent lamp installed after July 1998. Most of the lights were sold for commercial use, though some were sold for consumer use. This recall does not involve light fixtures containing incandescent or halogen lamps or fixtures with screw-in compact fluorescent lamps or straight tube (linear) fluorescent lamps.

CPSCAug 16, 2006Nationwide• Lutron Electronics Co. Inc., of Coopersburg, Pa.

Hitachi Medical Systems America Inc: MRP-7000 and AIRIS Magnetic Resonance Imaging Systems, So...

Image orientation error. When a 3D Maximum Intensity Projection (MIP) image data set is transferred from the MRI system to a computer workstation via the DICOM protocol, the anatomical markers do not change between the images as they rotate.

FDAAug 16, 2006Nationwide• Hitachi Medical Systems America Inc

Dell Notebook Batteries (Sony) – fire risk (2006)

Fire/Burn Risk

The recalled batteries were sold with or sold separately to be used with the following Dell notebook computers: Latitude™ D410, D500, D505, D510, D520, D600, D610, D620, D800, D810; Inspiron™ 6000, 8500, 8600, 9100, 9200, 9300, 500m, 510m, 600m, 6400, E1505, 700m, 710m, 9400, E1705; Dell Precision™ M20, M60, M70 and M90 mobile workstations; and XPS,™ XPS Gen2, XPS M170 and XPS M1710. "Dell" and one of the following markings are printed on the batteries: "Made in Japan," "Made in China," or "Battery Cell Made in Japan Assembled in China." The identification number for each battery appears on a white sticker.

CPSCAug 15, 2006Nationwide• Sony Energy Devices Corp., of Japan

Hitachi Medical Systems America Inc: Hitachi Echelon Magnetic Resonance Imaging System, Serial...

Component defect/overheating device; A malfunctioning decoupling circuit in the CTL coil caused high current flow and circuit overheating.

FDAAug 14, 2006Nationwide• Hitachi Medical Systems America Inc

Smiths Medical ASD, Inc.: Bivona Adult Tracheostomy Tube, Labeled I.D. 6.0 mm, O.D....

The length of the shaft is incorrectly stated as 7 mm, instead of the correct 17 mm, on the outer packaging, although the tray label is correct.

FDAAug 11, 2006Nationwide• Smiths Medical ASD, Inc.

Frameworx Chairs and Bar Stools (Brunswick) – unspecified risk (2006)

The recalled chairs and bar stools were sold under the model name Frameworx. The models affected are short table height chair model number 53-861025-000 and tall bar stool model number 57-860979-000. The model name and model numbers are not written on the chairs. The model number is only written on the original shipping carton, packing list or invoice. The chairs and bar stools have a plastic bucket-style seat bolted to a steel seat plate assembly that connects to the down tube of the seat.

CPSCAug 11, 2006Nationwide• Brunswick Bowling & Billiards Corp., of Lake Forest, Ill.

Respironics Novametrix, LLC.: NICO Model 7300 Cardiopulmonary Management System

Audible alarm may not sound during an alert condition

FDAAug 11, 2006PR• Respironics Novametrix, LLC.