Philips Electronics North America recalls

Philips Electronics North America has 160 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 19 Dec 2018. 7 are still ongoing.

Total recalls160since 2015

Last 12 months0reported

Class I00% of total

Ongoing7latest 19 Dec 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 158 99%Class III 2 1%

Why philips electronics north america is recalled

Product types

By year

20186843%
20172415%
20165736%
2015117%

Ongoing philips electronics north america recalls

7 active

Reported	Class	Recall	Company	Reason	Where
19 Dec 2018Device	CLASS II	IntelliVue MX40 Patient Monitor recalled by Philips Electronics North	Philips Electronics North America	Device Malfunction	Nationwide
29 Aug 2018Device	CLASS II	Philips SureSigns VS3 Vital Signs Monitor recalled	Philips Electronics North America	Device Malfunction	Nationwide
29 Aug 2018Device	CLASS II	Philips SureSigns VS2 monitor recalled by Philips Electronics North	Philips Electronics North America	Temperature Abuse	Nationwide
29 Aug 2018Device	CLASS II	Philips SureSigns VS4 Vital Signs Monitor recalled	Philips Electronics North America	Device Malfunction	Nationwide
29 Aug 2018Device	CLASS II	Philips SureSigns VSV (Vital Signs Viewer) recalled	Philips Electronics North America	Device Malfunction	Nationwide
29 Aug 2018Device	CLASS II	Philips SureSigns VM 3/4/6/8 Patient Monitors recalled	Philips Electronics North America	Temperature Abuse	Nationwide

All philips electronics north america recalls, newest first

160 total

Reported	Class	Recall	Company	Reason	Where
19 Dec 2018Device	CLASS II	IntelliVue MX40 Patient Monitor recalled by Philips Electronics North	Philips Electronics North America	Device Malfunction	Nationwide
24 Oct 2018Device	CLASS II	Philips HeartStart FR3 Defibrillator recalled	Philips Electronics North America	Sterility	Nationwide
3 Oct 2018Device	CLASS II	Allura Xper F010, System recalled by Philips Electronics North	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	Allura Xper FD2O Biplane, System recalled by Philips Electronics North	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	AIIuraXperFDlO, System recalled by Philips Electronics North	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	Integris Allura 9 F Fdxd, System recalled by Philips Electronics North	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	Integris Allura 15-12 (biplane), System recalled	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	AlluraXperFOlO/lO, System recalled by Philips Electronics North	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	Cesar-Dmcp-Visub(HM2000/3000), System recalled	Philips Electronics North America	Other	Nationwide
3 Oct 2018Device	CLASS II	Allura Xper F020 Biplane DR Table, System recalled	Philips Electronics North America	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.