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

DateAgencyProduct
October 3, 2018FDAINTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and neurovascular imaging…Z-3218-2018
October 3, 2018FDAAIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imag…Z-3230-2018
October 3, 2018FDAINTEGRIS CV, System Code 722030 Vascular, cardiovascular and neurovascular imaging ap…Z-3215-2018
October 3, 2018FDAAIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascu…Z-3231-2018
October 3, 2018FDAINTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular and neurovas…Z-3214-2018
October 3, 2018FDAAllura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imagi…Z-3221-2018
August 29, 2018FDAPhilips SureSigns VS4 Vital Signs Monitor, 863283 863286 The SureSigns VS4 vital sig…Z-2894-2018
August 29, 2018FDAPhilips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 86…Z-2895-2018
August 29, 2018FDAPhilips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of…Z-2892-2018
May 9, 2018FDAAllura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Int…Z-1589-2018
April 18, 2018FDAIntelliVue X3 Patient Monitor.Z-1315-2018
March 7, 2018FDAAllura Xper systems with Certeray X-ray Generator located in regions with high mains (480…Z-0716-2018
January 3, 2018FDAIntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue…Z-0292-2018
December 27, 2017FDAPhilips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environmen…Z-0268-2018
October 25, 2017FDAPhilips Healthcare Brilliance iCT X-Ray, Tomography, Computed These computed tomog…Z-0019-2018
June 21, 2017FDAPhilips DigitalDiagnost 3.1.x X-Ray SystemZ-2154-2017
June 21, 2017FDAM3150 Information Center Local Database; Models: 862249, 865001, 865003, 865004, 865007, …Z-2528-2017
June 21, 2017FDAPhilips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDia…Z-2322-2017
June 7, 2017FDANMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)Z-2175-2017
April 26, 2017FDAThe following systems are only affected if a Laird chiller is installed (11NC: 9896002159…Z-1822-2017
April 26, 2017FDAAllura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; All…Z-1820-2017
March 1, 2017FDAPhilips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central moni…Z-1229-2017
February 1, 2017FDAPhilips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Inf…Z-1106-2017
February 1, 2017FDAAllura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging a…Z-0924-2017
February 1, 2017FDAAllura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applic…Z-0923-2017

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.
What was the most recent Philips Electronics North America Corporation recall?
FDA recall Z-3218-2018, published October 3, 2018: INTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
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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