Philips Electronics North America Corporation
Andover, MA
This page shows every FDA and USDA recall linked to Philips Electronics North America Corporation. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
160
Total Recalls
2010
First Recall
2018
Most Recent
Philips X-Ray Systems, Allura Xper with R8.2.16
Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10...
Oct 1, 2015
· Device
Terminated
Philips HeartStart XL+ Defibrillator/Monitor
Product Usage:
The HeartStart XL+ is intended for use in a hospi...
Aug 4, 2015
· Device
Terminated
Invivo Expression MRI Patient Monitoring System.
Jul 27, 2015
· Device
Terminated
Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800220161, 45...
Jul 22, 2015
· Device
Terminated
Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for e...
Jul 22, 2015
· Device
Terminated
Philips Healthcare Ingenuity CT Computed Tomography X-ray system
Apr 14, 2015
· Device
Terminated
Philips Healthcare Ingenuity Core Computed Tomography X-ray system
Apr 14, 2015
· Device
Terminated
Philips Healthcare Brilliance 64 Computed Tomography X-ray system
Apr 14, 2015
· Device
Terminated
Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system
Apr 14, 2015
· Device
Terminated
Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1
Product Usage:
The Digi...
Mar 23, 2015
· Device
Terminated