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, Inc.

Philips Medical Systems, Inc. Recalls

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

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 12341–12360 of 17593 recalls

Lithium Polymer Battery (Philips Medical) – Battery Ignition (2014)

VCG battery ignited in a VCG unit when recharging.

Class IIModerate

FDANov 20, 2014AL, CA, FL +18 more• Philips Medical Systems, Inc.

Smoked Nova Salmon (Acme Smoked Fish) – listeria contamination (2014)

Listeria

Virginia Department of Agriculture and Consumer Services revealed the presence of Listeria monocytogenes in Smoked Nova Salmon.

Class IHigh

FDANov 20, 2014DE, MD, VA +1 more• Acme Smoked Fish Corp.

Whole Milk Yogurt (Flying Cow) – inadequate pasteurization (2014)

Flying Cow Creamery whole milk yogurt is recalled because the milk may not have been adequately pasteurized.

Class II

1...616 617618619 620...880

Page 618 of 880Next

Moderate

FDANov 20, 2014IN, WA• Flying Cow Creamery

IntelliVue TcG10 Monitor (Philips) – Contraindication Omission (2014)

Laceration Risk

Philips has discovered that the Instructions for Use (IFU) for the IntelliVue TcG10 Transcutaneous Gas Measurement Module is missing the contraindication that the device is not to be used on patients under gas anesthesia.

Class IIModerate

FDANov 19, 2014CA, HI, IL +8 more• Philips Medical Systems, Inc.

Semi-Auto Gun Bore Cleaner (Hoppe's) – child safety issue (2014)

This recall involves Hoppe's Semi-Auto Gun Bore Cleaner. This product is packaged in a brown 5-ounce plastic bottle with a blue and yellow label and black cap. The recalled item number is SA904 and can be found above the UPC code on the label.

CPSCNov 19, 2014Nationwide• TriPak Inc., Vandalia, Mich.

HeartStart MRx Monitor/Defibrillator (Philips) – Device Malfunction (2014)

Device may malfunction, which could cause therapy to be delayed, disabled, or delivered inadvertently.

Class IIModerate

FDANov 19, 2014Nationwide• Philips Medical Systems, Inc.

iTotal CR G2 Knee Replacement (ConforMIS) – Incorrect Serial Number (2014)

Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting

Class IIModerate

FDANov 19, 2014IN• ConforMIS, Inc.

Champion HCAC (Champion) – Adaptive Equipment (2014)

Champion Bus, Inc. (Champion Bus) is recalling certain model year 2006-2014 American Coach, American Crusader, Challenger, Corporal, Crusader, CTS-FE, CTS-RE, Defender, HCAC, HC American, Platinum Shuttle, and Stacked Rail transit buses manufactured January 1, 2006, to July 31, 2014, equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

NHTSANov 19, 2014Nationwide• CHAMPION

HeartStart MRx Monitor/Defibrillator (Philips) – CO2 Inlet Port (2014)

MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port associated with end-tidal carbon dioxide (EtCO2) monitoring on MRx Monitor/Defibrillators can be pushed into the MRx housing, making it inaccessible. 2. The handle can separate from the MRx housing due to breakage of mounts on the rear case.

Class IIModerate

FDANov 19, 2014Nationwide• Philips Medical Systems, Inc.

HeartStart MRx Monitor/Defibrillators (Philips) – Test and Capacitor Issue (2014)

1. Device will perform the weekly automated tests hourly, which could cause the therapy capacitors to degrade sooner than intended and 2. While connected to AC or DC power and with no battery installed or the battery installed has a charge level of less than 10%, the Ready for Use (RFU) indicator will not provide the expected low battery indication

Class IIModerate

FDANov 19, 2014Nationwide• Philips Medical Systems, Inc.

ECG Out Cable (Philips Electronics) – Signal Synchronization (2014)

When a Philips monitor/defibrillator is receiving an ECG signal from an auxiliary bedside monitor via a sync cable, the following can occur if the monitor/defibrillator experiences interference from electrical fast transients (EFTs) while connected to AC power: On the HeartStart MRx and HeartStart XL, EFT noise can be misinterpreted as an R-wave. On the HeartStart XL+, EFT noise can disable ECG monitoring, and potentially interrupt demand mode pacing.

Class IIModerate

FDANov 19, 2014Nationwide• Philips Electronics North America Corporation

Cool Draft Misting Fans (Ventamatic) – Fire and shock risk (2014)

Fire/Burn Risk

This recall involves Cool Draft misting mid-pressure and high-pressure misting fans. The misting fans fit on top of 15-gallon yellow or orange round Igloo coolers or on top of gray 40-gallon water tanks. Cool Draft by Ventamatic is printed on a sticker on the fan's water tank and www.cooldraft.com is printed on a sticker in the center of all of fans.

CPSCNov 13, 2014Nationwide• Ventamatic LTD, of Mineral Wells, Texas

ABX PENTRA Reagent Container (Horiba) – Rack Placement Issue (2014)

HORIBA Medical is recalling the ABX PENTRA 400 Reagent Container because they do not always sit properly into the reagent rack. In low reagent level scenarios, this could lead to insufficient reagent volume being pipetted and could lead to incorrect results being reported without an alarm. The defect would result in a false high or false low results for HbA1c and false high results for magnes

Class IIModerate

FDANov 13, 2014Nationwide• Horiba Instruments, Inc dba Horiba Medical

BrightView X (Philips) – Unintended Movement Risk (2014)

Unintended detector and gantry movement due to software issues.

Class IIModerate

FDANov 12, 2014Nationwide• Philips Medical Systems (Cleveland) Inc

Pediatric Urinary Catheters (Cure Medical) – Size Mislabeling (2014)

Laceration Risk

Some of the intermediate boxes within lot 140417-3, were labeled as P8, a French Size 8 pediatric catheter but actually contain P10, French Size 10 pediatric catheters. Trying to use a P10 catheter for bladder drainage, where P8 catheters have been prescribed, may result in acute urinary retention; and, forced attempts to insert the French Size 10 catheter lead to urethral trauma.

Class IIModerate

FDANov 11, 2014Nationwide• Cure Medical LLC

CareLink Pro (Medtronic) – Software Display Error (2014)

The firm is informing customers of a software error that might result in an inaccurate display of the Temp Basal time and duration in CareLink Clinical reports with data uploaded from the MiniMed 620G or 640G insulin pump.

Class IIILow

FDANov 10, 2014Nationwide• Medtronic MiniMed Inc.

truFreeze System (CSA Medical) – Timer Sound Loss (2014)

An increase in complaint trending for a loss of audible sound associated with the timer has been observed.

Class IIModerate

FDANov 10, 2014AR, CA, CO +22 more• CSA Medical

MEVION S250 (Mevion) – Dose Compensation Defect (2014)

Software defect that causes an incorrect dose compensation function to be applied to the internal dose ionization chamber when either pressure or temperature sensor malfunction. This could result in an incorrect dose delivery of no more than 5%.

Class IIModerate

FDANov 10, 2014IN, MO• Mevion Medical Systems, Inc.

IntelliSpace Portal (Philips) – Measurement Inaccuracy (2014)

Software defect. In certain circumstances, the application may display incorrect measurements of cardiac and aortic anatomy used to select and size the Transcatheter heart valve (THV) to be implanted .

Class IIModerate

FDANov 9, 2014FL, IN, NC +1 more• Philips Medical Systems (Cleveland) Inc

Radiotransparent Electrode (ConMed) – Connection Incompatibility (2014)

Philips Healthcare made changes to the design of the connection between multifunction electrodes and their HeartStart FR3 and HeartStart FRx AEDs. The failure to connect may result in a delay of therapy, which could result in patient death or serious injury.

Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation