How many recalls does Philips Electronics North America Corporation have?

Recalert has 44 U.S. recalls on record for Philips Electronics North America Corporation, published between September 2, 2015 and October 3, 2018.

Which agencies have handled Philips Electronics North America Corporation recalls?

Philips Electronics North America Corporation appears as the recalling firm in recalls from: FDA (44).

Philips Electronics North America Corporation: 44 recalls on record

Recalls filed with 1 agency: FDA (44).

First recall on record: September 2, 2015. Most recent: October 3, 2018.

Risk classification: Class II: 43 · Class III: 1

Most recent recalls

Date	Agency	Product	Recall number
February 1, 2017	FDA	Velara Generator with an old Firmware version used with the Philips Integris BH5000Z-1062-2017	Z-1062-2017
November 30, 2016	FDA	Philips Healthcare System X-ray Tomography Computed :Z-0376-2017	Z-0376-2017
March 16, 2016	FDA	Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O a…Z-1066-2016	Z-1066-2016
March 9, 2016	FDA	SENSE Body Coil 1.5T with identification; used in the ACS NT, Intera 1.5T and Achieva 1.…Z-1024-2016	Z-1024-2016
March 2, 2016	FDA	Philips Healthcare IntelliVue Info Center iX, A.0 866023Z-0856-2016	Z-0856-2016
March 2, 2016	FDA	Philips Healthcare IntelliVue Info Center iX, B.0, 866389 Physiological, Patient Monit…Z-0858-2016	Z-0858-2016
March 2, 2016	FDA	Philips Healthcare PIIC Classic Upgrade, 866117 Physiological, Patient Monitor (With Ar…Z-0857-2016	Z-0857-2016
February 17, 2016	FDA	Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological e…Z-0766-2016	Z-0766-2016
February 10, 2016	FDA	Allura Xper FD10, FD10 C, and FD10 F; Model Numbers: 722026 722010 722003 722002 722001 …Z-0702-2016	Z-0702-2016
February 10, 2016	FDA	INTEGRIS BH3000; Model Number: 72242 The Philips INTEGRIS 3000 I 5000 system is intend…Z-0720-2016	Z-0720-2016
February 10, 2016	FDA	Allura Xper FD10/10; Model Numbers: 722027 722011 722005 Intended for Cardiovascular a…Z-0703-2016	Z-0703-2016
February 10, 2016	FDA	INTEGRIS V3000; Model Number: 72243, 72244, 72245 The Philips INTEGRIS 3000 I 5000 sys…Z-0721-2016	Z-0721-2016
February 10, 2016	FDA	INTEGRIS BH5000; Model Number: 72247 The Philips INTEGRIS 3000 I 5000 system is intend…Z-0723-2016	Z-0723-2016
February 10, 2016	FDA	INTEGRIS CV; Model Number: 722030 The Philips INTEGRIS 3000 I 5000 system is intended …Z-0729-2016	Z-0729-2016
February 10, 2016	FDA	Allura Xper FD20 Biplane; Model Numbers: 722013 722008 722015 Dedicated vascular and n…Z-0711-2016	Z-0711-2016
February 10, 2016	FDA	Allura Xper FD20/10; Model Numbers: 722029 Dedicated vascular and neurovascular imagin…Z-0705-2016	Z-0705-2016
February 10, 2016	FDA	INTEGRIS H5000; Model Number: 72246 The Philips INTEGRIS 3000 I 5000 system is intende…Z-0722-2016	Z-0722-2016
December 23, 2015	FDA	Philips Healthcare Ingenuity Core Computed Tomography X-ray systemZ-0406-2016	Z-0406-2016
September 2, 2015	FDA	Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 …Z-2383-2015	Z-2383-2015

Questions about this company

How many recalls does Philips Electronics North America Corporation have?: Recalert has 44 U.S. recalls on record for Philips Electronics North America Corporation, published between September 2, 2015 and October 3, 2018.
Which agencies have handled Philips Electronics North America Corporation recalls?: Philips Electronics North America Corporation appears as the recalling firm in recalls from: FDA (44).

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Philips Electronics North America Corporation: 44 recalls on record

Most recent recalls

Questions about this company

Do you carry products from Philips Electronics North America Corporation? Check your whole catalog free against 80,000+ recalls.

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