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Philips Medical Systems, Inc.

Philips Medical Systems, Inc. Recalls

All product recalls associated with Philips Medical Systems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

579

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 7661–7680 of 10937 recalls

Philips Medical Systems, Inc.: Patient Support Material Number: 9890 010 87431 used with...

The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.

Class IIModerate

FDAAug 19, 2014AZ, CT, FL +9 more• Philips Medical Systems, Inc.

Hitachi Medical Systems America Inc: Hitachi Echelon Oval MRI system is a diagnostic imaging d...

Fire/Burn Risk

The Gradient Coil was found to have a failure mode that allowed it to overheat and become a burn hazard.

Class IIModerate

FDAAug 18, 2014Nationwide• Hitachi Medical Systems America Inc

Varian Medical Systems, Inc.: 4D Integrated Treatment Console (4DITC), versions 10 and ...

Due to user error, the 4DITC can improperly allow users to clear a safety interlock imposed by the 4DITC on behalf of Varian's Bar Code Conical Verification system from the BrainLab's ExacTract console when it is used with BCCV.

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Class IIModerate

FDAAug 18, 2014Nationwide• Varian Medical Systems, Inc.

Oil Free Original Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Original Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari," Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Roots Thai Coconut Curry Hummus (Roots Organic) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Lima Bean Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Black Bean Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Roasted Red Pepper Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Spinach Hummus (Roots Organic Gourmet) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Roots Hot Chipotle Hummus (Roots Organic) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Thien Minh Cashew Kernels (Specialty Commodities) – Salmonella Risk (2014)

Salmonella

The Cashew Pieces have the potential to be contaminated with Salmonella.

Class IHigh

FDAAug 15, 2014CO, NJ• Specialty Commodities, Inc.

Roots Roasted Garlic Hummus (Roots Organic) – Undeclared Soy (2014)

Although ingredient statement lists "Tamari", Label lacks statement, "Contains Soy."

Class IIModerate

FDAAug 15, 2014CA, GA, NH +3 more• Roots Organic Gourmet

Snowmobiles (Arctic Cat) – Fuel Leak Fire Risk (2014)

Fire/Burn Risk

This recall involves model year 2014 Arctic Cat XF 7000 and ZR 7000 and model year 2015 XF 7000 and ZR 7000 snowmobiles. They were sold in a variety of green, black, orange and white color combinations. All XF and ZR 2014 models are included in this recall. Recalled 2015 model vehicles have the last six digits of the vehicle identification number (VIN) in the following ranges: 100920 through 100993 for the XF 7000 models and 100792 through 100919 for the ZR 7000. The fourth and fifth digits of the VIN, "14" or "15," correspond to the model year. The VIN appears on a sticker attached to the chassis near the rider's right foot rest. The model name appears on the front sides of the snowmobile.

CPSCAug 14, 2014Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Smoke Detectors (Fyrnetics) – Failure to Alert (2014)

Fire/Burn Risk

This recall involves thirty-three models of the 400 and 500 series Edwards (ESL)-branded and Interlogix smoke detectors hard-wired into a security system. Edwards and Interlogix smoke detectors are identical. The 2-wire or 4-wire detectors are round, white and measure 6 inches across by 2 inches high. The smoke detectors were made for professional installation and used primarily in commercial buildings, schools, hotels/motels, apartments, dormitories and homes as part of the fire alarm system. Recalled units have date codes 13084 through 14059 with the first two digits representing the year, for example: 13 for 2013 and 14 for 2014; and the last three digits representing the day of the year, for example: 084 is the 84th day of 2013, which is March 25, 2013. The initials ESL, the date code and one of the following model numbers are printed on a label on the back of the detector's cover and on the product's packaging. 400 series: 429AT, 429C, 429CAD, 429CRT, 429CST, 429CT, 429CTAD, 449AT, 449C, 449CRT, 449CSRH, 449CSRT, 449CST, 449CSTE, 449CT and 449CTE. 500 Series: 511C, 518C, 521B, 521BXT, 521B-10PKDMP, 521B-10PKG, 521BXT-10PKG, 521BXT-DMP-10PKG, 528B, 528CRXT, 541C, 541C-10PKG, 541CXT, 541CXT-10PK and 548C.

CPSCAug 13, 2014Nationwide• Fyrnetics Limited of Hong Kong, China

Ground Oregano (McCormick) – Salmonella Contamination (2014)

Salmonella

Retail sample of ground oregano tested positive for Salmonella.

Class IHigh

FDAAug 13, 2014AL, AZ, CA +36 more• McCormick & Company, Inc.

Horiba Instruments, Inc dba Horiba Medical: ABX PENTRA Magnesium RTU Reagent, Part No. A11A01646 P...

Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the on-board stability claims has been updated. Horiba has updated the ABX PENTRA Magnesium RTU package inserts by removing the 7-day on-board stability claim and replacing it with a 1-day on-board stability claim.

Class IIModerate

FDAAug 11, 2014Nationwide• Horiba Instruments, Inc dba Horiba Medical

ELITech Clinical Systems SAS: ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255,...

Some users of ENVOY 500 AST Reagent Kit, reference 55255, for Envoy 500 systems are observing that Quality Control (QC) fails before the product expiry is reached.

Class IIILow

FDAAug 11, 2014Nationwide• ELITech Clinical Systems SAS

Philips Medical Systems, Inc.: Philips Healthcare Integris Allura 15 -12 Fluoroscopy x...

Philips had discovered through a field service testing where a device failed to comply with a Federal standard.

Class IIModerate

FDAAug 8, 2014FL• Philips Medical Systems, Inc.

Philips Medical Systems, Inc.: Philips IntelliSpace ECG Management System, with softwar...

Philips IntelliSpace ECG (IECG) Management Systems that are importing Stress ECG records from a Quinton Stress ECG system have the potential for the patient record to contain multiple and therefore inaccurate patient identifiers such as: patient name, patient ID (PID), Medical record number (MRN). This creates the potential for misdiagnosis and incorrect therapy.

Class IIModerate

FDAAug 7, 2014CA, GA, NH +3 more• Philips Medical Systems, Inc.