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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

1000

Class I (Serious)

127

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 18741–18760 of 25002 recalls

MR Systems (Philips) – Image Order Reversal (2014)

When a fused series of a sagittal, coronal or radial multi station scan is generated in MobiView, the resultant image order is reversed. This occurs with software release R5.1.7/R5.1.8.

Class IIModerate

FDAAug 21, 2014Nationwide• Philips Medical Systems, Inc.

Hercules Stabilizing Arm (Terumo) – Pin Failure Risk (2014)

Terumo Cardiovascular Systems (Terumo CVS) is recalling certain lots of Hercules TM 360 Universal Stabilizing Arms because the two pins that hold the sleeve attached to the distal end of the device may come loose, causing the pins and sleeve to separate from the device. While the arm can still function without the pins and sleeve in place, there is potential for the loose components to fall into the surgical site.

Class IIModerate

FDAAug 20, 2014Nationwide• Terumo Cardiovascular Systems Corporation

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Ellipse Defibrillators (St Jude) – High Voltage Therapy Risk (2014)

An anomaly may result in delayed, partial, or no delivery of high voltage therapy. Internal damage to the high voltage capacitors, which may result in extended charge time, occurring during capacitor maintenance or charging for high voltage therapy. It may present as a vibratory patient notification and upon interrogation, a programmer or Merlin.net alert.

Class IIModerate

FDAAug 19, 2014Nationwide• St Jude Medical Cardiac Rhythm Management Division

Patient Support (Philips) – Footplate Fall Risk (2014)

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.

Patient Support (Philips) – Footplate Fall Risk (2014)

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.

Echelon Oval MRI (Hitachi) – Gradient Coil Burn Risk (2014)

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

4D Treatment Console (Varian) – Safety Interlock Issue (2014)

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.

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)

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

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

SAM Junctional Tourniquet (Sam Medical) – Snap Hook Failure (2014)

SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112, is recalled because the snap hook on auxiliary strap broke during training demonstration.

Class IIModerate

FDAAug 14, 2014Nationwide• Sam Medical Products

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

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.

Precision Flow Circuit (Vapotherm) – Water Lumen Leak (2014)

Disposable Patient Circuit that allows water to leak into the center gas lumen

Class IIModerate

FDAAug 13, 2014Nationwide• Vapotherm, Inc.