PlainRecordsBrand recall history
Advanced Neuromodulation Systems recalls
Every FDA recall record we found for Advanced Neuromodulation Systems, newest first. Updated Oct. 11, 2026.
9
9 recalls since 2009. The most recent was on March 6, 2013.
- Last 12 months
- 0
- Most recent
- 2013-03
- Most serious (FDA Class I)
- 0
- Last 30 days
- 0
Recalls by year
2012–2026121314151617181920212223242526
Class I (FDA, most serious)Other recalls
All recalls
9- March 6, 2013Advanced Neuromodulation Systems… Class IIUnintended Fluid ingress into the device header has been shown.
- Oct. 17, 2012The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel… Class IIEon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden, brief surge in stimulation that would be felt by the patient as…
- Sept. 5, 2012Eon (Model 3716) IPG is a dual channel… and 1 more product Class IIAs of 11/30/2011, St. Jude Medical has received 110 patient complaints of warmth or heating at the implantable pulse generators (IPGs) implant site…
- July 18, 2012Eon Mini Neurostimulation (IPG) System (Model 3788)… Class IIThe firm has received 112 complaints of the Eon Mini IPGs that lost the ability to communicate or recharge due to a workmanship issue resulting in…
- Aug. 30, 2011Software version 3.3 for Rapid Programmer devices… Product programmed with unapproved software was distributed.
- June 22, 2011Eon Mini Neurostimulation (IPG) System Model 3788 System is indicated as an aid in the management of chronic… Defective battery was identified as cause for reports of inability to communicate or recharge the product.
- May 13, 2010Eon Mini Implantable Pulse Generator (IPG)… Due to a missed inspection step during manufacturing, a small number of devices may experience a gradual or sudden loss of charging capability.
- April 21, 2010Swift-Lock (TM) Anchor Accessory Kit… Directions For Use of product incorrectly stated lead compatibility information.
- Nov. 10, 2009Eon Rechargeable Implantable Pulse Generator (IPG) System Product's external charging system on occasion was failing to communicate with the Implantable Pulse Generator preventing re-charging of the pain…
No recalls match.
How we match: a recall is listed here when the agency names Advanced Neuromodulation Systems as the company that filed it. Sources: FDA enforcement reports and FDA-posted company announcements, CPSC recall notices and NHTSA recall campaigns.