Recalls in 2017

Every food, drug and medical device recall reported to the FDA and USDA in 2017.

Recalls7,004in this period

Food3,348FDA + USDA

Drugs1,073FDA

Class I1,368most serious

Breakdown

Devices: 2,583

Class I 1,368 20%Class II 5,177 74%Class III 449 6%Other/pending 10

7,004 total

Reported	Class	Recall	Company	Reason	Where
27 Dec 2017Device	CLASS II	Etest Oxacillin OX 256 WW F100 In vitro diagnostic recalled	BioMerieux	Packaging Defects	Nationwide
27 Dec 2017Device	CLASS II	Automated External Defibrillator recalled by Philips Electronics North	Philips Electronics North America	Other	MA
27 Dec 2017Device	CLASS II	Terumo(R) Overpressure Safety Valve recalled	Terumo Cardiovascular Systems	Other	MD
27 Dec 2017Device	CLASS II	ExploR Radial Head Replacement System recalled by Zimmer Biomet	Zimmer Biomet	Packaging Defects	IN
27 Dec 2017Device	CLASS II	Instrument Kit System, Tapered Screw-Vent Implant System recalled	Zimmer Dental	Other	Nationwide
27 Dec 2017Device	CLASS II	Azurion 3 M12, Azurion 3 M15, Allura R9 7 M12 recalled	Philips Electronics North America	Foreign Material	Nationwide
27 Dec 2017Device	CLASS II	Xper Flex Cardio Physiomonitoring system recalled by Invivo	Invivo	Other	49 states
27 Dec 2017Device	CLASS II	I-125 CE Marked QuickLink Cartridges recalled by C.R. Bard	C.R. Bard	Other	GA
27 Dec 2017Device	CLASS II	Rezum System, Vapor BPH Ablation System recalled by Nxthera	Nxthera	Device Malfunction	19 states
27 Dec 2017Device	CLASS II	Instrument Kit System, Tapered Screw-Vent Implant System recalled	Zimmer Dental	Other	Nationwide