Philips Medical Systems, Inc. recalls

29 recalls on record · latest: April 23, 2015

Official U.S. recall history for Philips Medical Systems, Inc., compiled from official government records.

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Philips Medical Systems, Inc. recalls Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP software allows qualified medica…

April 23, 2015 · Medical device recalls Moderate risk A problem (the dose computed in planning mode is calculated incorrectly ) has b…

Philips Medical Systems, Inc. recalls Philips Healthcare DigitalDiagnost System X-Ray

February 9, 2015 · Medical device recalls Moderate risk The system is designed to emit a beep upon termination of an exposure. However,…

Philips Medical Systems, Inc. recalls Philips Healthcare DuraDiagnost X- Ray

February 9, 2015 · Medical device recalls Moderate risk The system is designed to emit a beep upon termination of an exposure. However,…

Philips Medical Systems, Inc. recalls Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage: The Allura Xper series is intended for use in…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product Usage: The Allura Xper series is intended for use…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage: The Allura Xper series is intended for use i…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper FD10/10 Allura Xper FD20 Allura Xper FD21 Allura Xp…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare INTEGRIS cardio system Model : 722121 Product Usage: The Allura Xper series is intended for use in c…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Xper vascular system Model : 722124 Product Usage: The Allura Xper series is intended for use in car…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Usage: The Allura Xper series is intended for use in…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Xper cardio systems Model : 722123 Product Usage: The Allura Xper series is intended for use in card…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20 BIPLANE R7.6 722013 Allura Xper FD20 BIPLANE R7…

February 3, 2015 · Medical device recalls Moderate risk Monitor Ceiling Suspension system may fall

Philips Medical Systems, Inc. recalls Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211

January 23, 2015 · Medical device recalls Moderate risk Improper installation of Tube arm, and Wall stand may cause it to fall down, Im…

Philips Medical Systems, Inc. recalls HeartStart MRx monitor/defibrillator Models M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6…

December 23, 2014 · Medical device recalls Moderate risk MRx monitor/defibrillator could reboot at an indeterminate time, potentially ca…

Philips Medical Systems, Inc. recalls Philips IntelliVue Information Center iX (release A.00, A.01, and A.02) are impacted by this issue: 866023 IntelliVue I…

December 19, 2014 · Medical device recalls Moderate risk Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled withou…

Philips Medical Systems, Inc. recalls Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…

November 20, 2014 · Medical device recalls Moderate risk VCG battery ignited in a VCG unit when recharging.

Philips Medical Systems, Inc. recalls HeartStart MRx Monitor/Defibrillator; Model. Numbers: M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M…

November 19, 2014 · Medical device recalls Moderate risk Device may malfunction, which could cause therapy to be delayed, disabled, or d…

Philips Medical Systems, Inc. recalls Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of t…

November 19, 2014 · Medical device recalls Moderate risk Philips has discovered that the Instructions for Use (IFU) for the IntelliVue T…

Philips Medical Systems, Inc. recalls Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A

November 19, 2014 · Medical device recalls Moderate risk 1. Device will perform the weekly automated tests hourly, which could cause the…

Philips Medical Systems, Inc. recalls Philips HeartStart MRx Monitor/Defibrillator Models:M3535A, M3536A, M3536M, M3536MC, M3536M4, M3536M5 The HeartStart MR…

November 19, 2014 · Medical device recalls Moderate risk MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port assoc…

Philips Medical Systems, Inc. recalls Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 This Philips Mult…

September 24, 2014 · Medical device recalls Moderate risk Loss of key image functionality due to a bent pedal of the Footswitch.

Philips Medical Systems, Inc. recalls Foot Switches used with the following systems: Philips Allura Xper Systems; 722001 AlluraXperFDlO C, 722002 Allura Xper…

September 24, 2014 · Medical device recalls Moderate risk Loss of key image functionality due to a bent pedal of the Footswitch.

Philips Medical Systems, Inc. recalls Ingenia, Intera, Achieva and Achieve dStream MR systems on Software versions R5.1.7 and R5.1.8 with the Mobi View softw…

August 21, 2014 · Medical device recalls Moderate risk When a fused series of a sagittal, coronal or radial multi station scan is gene…

Philips Medical Systems, Inc. recalls Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037

August 19, 2014 · Medical device recalls Moderate risk The hook does not securely hold the footplate in vertical position. Therefore t…

Philips Medical Systems, Inc. recalls Patient Support Material Number: 9890 010 87431, used with:EasyDiagnost ; Model: 706050

August 19, 2014 · Medical device recalls Moderate risk The hook does not securely hold the footplate in vertical position. Therefore t…

Philips Medical Systems, Inc. recalls Philips Medical System Allura Xper X-Ray Angiographic

June 6, 2014 · Medical device recalls Moderate risk In certain circumstances, a software error can lead to a situation where the fi…

Philips Medical Systems, Inc. recalls All Philips Ingenia, Intera, Achieva and Multiva MR systems using R5.1i and R5.1 .2 version of software. Indicated for…

May 5, 2014 · Medical device recalls Moderate risk In spine clinical workflows, cross reference lines may be used to determine the…

Philips Medical Systems, Inc. recalls Philips Multi Diagnost Eleva II

October 14, 2013 · Medical device recalls Moderate risk The possibility of the Reference Air Kerma Rate for low dose mode will not be r…

Philips Medical Systems, Inc. recalls Philips Multi Diagnost Eleva with FlatDetector

October 14, 2013 · Medical device recalls Moderate risk The possibility of the Reference Air Kerma Rate for low dose mode will not be r…