Advanced Neuromodulation Systems recalls

Advanced Neuromodulation Systems has 5 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 6 Mar 2013.

Total recalls5since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 Mar 2013

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 5 100%Class III 0 0%

Why advanced neuromodulation systems is recalled

Other Reasons360%
Device Malfunction240%

Product types

Other Medical Devices5100%

By year

2013120%
2012480%

All advanced neuromodulation systems recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
6 Mar 2013Device	CLASS II	Brio DBS System implantable neurostimulator, IPG or R-ipg recalled	Advanced Neuromodulation Systems	Other	TX
17 Oct 2012Device	CLASS II	The Eon Mini Implantable Pulse Generator recalled	Advanced Neuromodulation Systems	Device Malfunction	Nationwide
5 Sep 2012Device	CLASS II	Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed recalled	Advanced Neuromodulation Systems	Other	Nationwide
5 Sep 2012Device	CLASS II	The Eon Mini Neurostimulation (IPG) System recalled	Advanced Neuromodulation Systems	Other	Nationwide
18 Jul 2012Device	CLASS II	Eon Mini Neurostimulation (IPG) System recalled	Advanced Neuromodulation Systems	Device Malfunction	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.