Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St. Jude Medical Due to St. Jude Medical has informed your doctor that...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact St. Jude Medical directly.
Affected Products
Eon Mini - 3721 (Charger). Product Usage: Eon Mini system is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, intractable low back and leg pain.
Quantity: 70,638 (combined total of the Eon and the Eon Mini systems)
Why Was This Recalled?
St. Jude Medical has informed your doctor that a number of cases have been reported in which discomfort associated with heating occurred at the device site while patients were using the Charging System to charge their spinal cord stimulator. In three cases, patients received a burn to the skin (one second-degree and two first-degree burns) at the implant site. As of June 30, 2012, St. Jude Medica
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About St. Jude Medical
St. Jude Medical has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report