Cyberonics recalls

Cyberonics has 9 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 27 Jun 2018. The most frequent reason is device malfunction.

Total recalls9since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 27 Jun 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 9 100%Class III 0 0%

Why cyberonics is recalled

Product types

Other Medical Devices9100%

By year

2018222%
2017222%
2016222%
2015222%
2014111%

All cyberonics recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
27 Jun 2018Device	CLASS II	VNS Therapy Programmer recalled by Cyberonics	Cyberonics	Lead & Heavy Metals	21 states
14 Feb 2018Device	CLASS II	VNS(R) Therapy Programmer, GMDN recalled by Cyberonics	Cyberonics	Device Malfunction	CO, ND
23 Aug 2017Device	CLASS II	VNS Therapy¿ AspireHC¿ Generator recalled by Cyberonics	Cyberonics	Other	Nationwide
23 Aug 2017Device	CLASS II	VNS Therapy¿ AspireHC¿ Generator recalled by Cyberonics	Cyberonics	Other	Nationwide
27 Jan 2016Device	CLASS II	Vagus Nerve Stimulator VNS Therapy AspireSR Generator recalled	Cyberonics	Device Malfunction	Nationwide
27 Jan 2016Device	CLASS II	VNS Therapy AspireSR Generator recalled by Cyberonics	Cyberonics	Other	TX
25 Nov 2015Device	CLASS II	Vagus Nerve Stimulator (VNS) Therapy AspireSR Generator recalled	Cyberonics	Device Malfunction	17 states
6 May 2015Device	CLASS II	VNS Therapy DemiPulse Generator recalled by Cyberonics	Cyberonics	Device Malfunction	9 states
31 Dec 2014Device	CLASS II	VNS Therapy AspireHC recalled by Cyberonics	Cyberonics	Lead & Heavy Metals	PA

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.