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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

620

Class I (Serious)

Most Recent

Dec 2025

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 10221–10240 of 10937 recalls

Philips Medical Systems North America Co. Phillips: AD6 table, modified, used with the XPER systems. The mo...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD6 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD5 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

1...510 511512513 514...547

Page 512 of 547Next

FDA

Oct 12, 2005

Nationwide

• Philips Medical Systems North America Co. Phillips

Toshiba American Med Sys Inc: Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonan...

To correct a hardware problem of water leakage in the cooling system inside the ASGC, leading to the replacement of the gradient coil.

FDAOct 12, 2005Nationwide• Toshiba American Med Sys Inc

Philips Medical Systems North America Co. Phillips: AD5 table, modified, used with the XPER x-ray systems. ...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 6 inch diameter Rolle...

Six inch roller pumps were mislabeled as 4 inch roller pumps.

FDAOct 6, 2005MI• Terumo Cardiovascular Systems Corp

Reebok Children's Fleece Set – Potential Safety Issue (2005)

Choking Hazard

Only Reebok fleece pullover/pant sets with navy blue quarter-zip zippers are being recalled. The fleece pullover/pant sets were sold in navy blue/red and navy blue/pink in sizes up to children's size 7. "Reebok" is printed across the front of the pullover. The pullovers have a hood that can be folded under the collar. Some of the recalled pullovers were sold with matching mittens. The style numbers were printed on the store tag only and end in: 1816, 2816, 3816, 1816N, 2816N, 1814, 2814, 4814, and 5814.

CPSCOct 6, 2005Nationwide• Adjmi Apparel Group, of New York, N.Y. (Adjmi is an authorized licensee of children's apparel products of Reebok, of Canton, Mass.)

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 4 inch diameter Rolle...

An incorrect serial number was placed on one roller pump.

FDAOct 6, 2005MI• Terumo Cardiovascular Systems Corp

Misys Healthcare Systems: Misys Laboratory version 6.1 - Microbiology Module

Customer complaint during testing of module prior to production use. Software problem when the user has indicated to enter a coded comment instead of using the defined keyboard, then enters 100,000, the system willfile the number 100 instead of number 100,000.

FDASep 29, 2005Nationwide• Misys Healthcare Systems

General Electric Med Systems LLC: Sopha Medical Vision DST / DST-XL Digital vatiable angle ...

Cracked welds on the main rotation shaft could potentially lead to the collapse of the gantry yokes that support the detectors if the system is continued to be used after the weld has completely fractured.

FDASep 27, 2005AL, AZ, CA +19 more• General Electric Med Systems LLC

Arctic Cat Prowler XT Utility Vehicle – Mechanical Risk (2005)

The Prowler XT was produced in three colors: Green, Cat Green, and Red. The vehicles have the words Arctic Cat on each side of the cargo box, 650 H1 on each side of the front hood, and the name Prowler XT centered on the front of the hood. The recalled units fall within the vehicle identification range (VIN) of 4UF06MPV06T300001 through 4UF06MPV86T300781. Consumers only need to look at the final six digits of the VIN to determine if their vehicle is included in this recall. Model Number of Affected Models Model Model Number Prowler XT Green U2006P2S4BUSG Prowler XT Cat Green U2006P2S4BUSZ Prowler XT Red U2006P2S4BUSR

CPSCSep 22, 2005Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Rita Medical Systems: Rita Brand Habib 4X Electrosurgical Coagulator, Catalog N...

Devices for which sterility may be compromised as evidenced by a loss of package integrity.

FDASep 21, 2005Nationwide• Rita Medical Systems

Toshiba American Med Sys Inc: High voltage generator XTP-8100G and XTPG-8100G for the I...

It was found during a study, arcing might occur in the transformer of the high voltage generator, XTP-8100G and XTBP-8100G displaying an error message and interrupting fluoroscopy.

FDASep 21, 2005CA, CO, IL +11 more• Toshiba American Med Sys Inc

Varian Medical Systems Oncology Systems: Varis Vision Treatment 6.6/RTP Exchange/Siemens Accelerators

A software anomaly may occur which can lead to patient treatment with the wrong field. The anomaly is reported only to occur when this software version (6.6.5022) is used with Elekta or Siemens linear accelerators .

FDASep 20, 2005AZ, CA, IN +4 more• Varian Medical Systems Oncology Systems

Medical Components, Inc dba MedComp: Jet Medical 4F x 60cm Single Lumen Polyurethane PICC Nurs...

The product is labelled as containing a 4F catheter when the trays/kits actually contain a 5F catheter. The catheters will not fit into the sheath-dilator that was included in the tray. mislabeled as 4F

FDASep 15, 2005IN, MO, OH• Medical Components, Inc dba MedComp

Bottle Sippers Pull-Up Caps (Bradshaw) – Potential Safety Issue (2005)

Choking Hazard

The recalled bottle sippers have white screw-on bases with dark blue, green or red pull-up valves. They are sold in packages of three. The package is labeled "Bottle Sippers." Bradshaw International Inc. and #70118 are written on the back of the package.

CPSCSep 15, 2005Nationwide• Bradshaw International Inc., of Rancho Cucamonga, Calif.

Medical Components, Inc dba MedComp: Jet Medical 4F Single Lumen PICC Kit. Catalog number JP7-4

FDASep 15, 2005IN, MO, OH• Medical Components, Inc dba MedComp

Terumo Cardiovascular Systems Corp: Terumo Sarns brand Flexible arterial cannula, 7.5 mm (22 ...

There may be a solvent bond failure at the tubing/connector site of the cannula, resulting in the disconnection of the cannula parts.

FDASep 12, 2005Nationwide• Terumo Cardiovascular Systems Corp

Medtronic Emergency Response Systems, Inc.: standard (hard) paddles used with the LIFEPAK 12 defibril...

Potential for voltage pins in connector of therapy cable to break.

FDASep 2, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Merit Medical Systems, Inc: Merit Custom Procedure Kit

Component of procedure kits may allow higher than desired amount of IV solution to be infused in to patient during pressure monitoring procedure.

FDASep 2, 2005MD, OR, VA +1 more• Merit Medical Systems, Inc