Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
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.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16541–16560 of 17592 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...826 827828829 830...880

Page 828 of 880Next

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

Advanced Medical Optics, Inc.: CeeOn EDGE Silicone Posterior Chamber IOLs (Modelsl 911A ...

A small opening (channel or tunnel) in the seal of the outer Tyvek pouch which contains the lens case, in which the sealed intraocular lens is packaged may not be adequately sealed, therefore the potentially compromised outer Tyvek pouch may not be sterile and may potentially contaminate an otherwise sterile field during surgery.

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: Tecnis Monofocal Silicone Posterior Chamber IOLs (Models:...

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Poste...

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: Tecnis Multifocal Silicone Posterior Chamber IOLs (Model:...

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: CeeOn Heparin SurfaceModifie (HSM) PMMA One-Piece Anterio...

FDAOct 5, 2005Nationwide• Advanced Medical Optics, Inc.

Dakocytomation California Inc: K 520411-2, Hercep Test, 35Test, HER2, Protein

Formulation error in the Visualization Reagent (vial 3) component contained in Hercep Test kits. The error was in the concentration of Polyethylene Glycol contained in the formulation.

FDASep 29, 2005Nationwide• Dakocytomation California Inc

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

Dakocytomation California Inc: K 520711-2, Hercep Test, 35Test, HER2, Protein

Formulation error in the Visualization Reagent (vial 3) component contained in Hercep Test kits. The error was in the concentration of Polyethylene Glycol contained in the formulation.

FDASep 29, 2005Nationwide• Dakocytomation California Inc

Wood Company Freezers – Potential Safety Issue (2005)

Fire/Burn Risk

The recalled single-door freezers and refrigerators are 15-, 17- and 20-cubic-foot Automatic Defrost Upright Freezers and 17-cubic-foot Automatic Defrost All-Refrigerators that can be converted into freezers. They were sold under the brand names Amana, Crosley, Danby, Maytag, Whirlpool and Wood's, which is written on the front of the unit. The manufacturer label with the model number and date of manufacture is located on the inside of the cabinet. A list of model numbers and dates of manufacture included in the recall follows: Brand Model Numbers Date of Manufacture Amana AFU1567*, AFU1767*, AFU2067* 200209(September 2002)through200402(February 2004) Crosley FFCR17*, WCF15*, WCF17*, WCF20* Danby DUF1700*, DFF1708* Maytag MQU1556*, MQU2057* Whirlpool EV150NXM*, EV170NYL*, EV171NYM*, EV200NXK*, EV201NXM*, EL7ATRRK*, EL7ATRRM*, EL7JWKLM*, EL7JWKRM* Wood's F15*, F17*, F20*, F42*, F47*, F55*, WFF15*, WFF17*, WFF20*,RFA17*, RFC17*, R47F* *there are additional letters or numbers following the model numbers above

CPSCSep 27, 2005Nationwide• W.C. Wood Company Inc., of Ottawa, Ohio

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