Abbott Medical recalls Liberta RC DBS IPG
- Recalling company
- Abbott Medical
- Product
- Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400
- Reason
- There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC).
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 6, 2025
- Reported
- Nov 19, 2025
- Distribution
- Worldwide distribution.
- Status
- Ongoing
- Quantity
- 722 units
- Lot / codes
- UDI/DI 05415067047663, Serial Numbers: 20196493, 20196495, 20196496, 20196497, 20196498, 20196500, 20196502, 20196503, 20196504, 20196505, 20196506, 20196507, 20196508, 20196509, 20196511, 20196512, 20196513, 20196514, 20196515, 20196516, 20196517, 20207397, 20207398, 20207399, 20207400, 20207401, 20207402, 20207403, 20207405, 20207406, 20207407, 20207408, 20207409, 20207410, 20207411, 20207412, 20207413, 20207414, 20207415, 20207416, 20207417, 20207418, 20207419, 20207420, 20207421, 20207422, 20207423, 20207424, 20207425, 20207427, 20207428, 20207429, 20207430, 20207431, 20207432, 20207433, 20207434, 20207435, 20207436, 20207437, 20207438, 20207441, 20207442, 20207443, 20207444, 20207445, 20207446, 20207447, 20207448, 20207449, 20207450, 20207451, 20207452, 20207454, 20207455, 20207456, 20207457, 20207458, 20207459, 20207460, 20207461, 20207462, 20207463, 20207464, 20207465, 20207466, 20207467, 20207468, 20207469, 20207470, 20207471, 20207472, 20207473, 20207474, 20207477, 20207478, 20207481, 20207482, 20207483, 20207484, 20207485, 20207486, 20207487, 20207488, 20207489, 20207490, 20207491, 20207494, 20207495, 20207496, 20208681, 20208682, 20208683, 20208684, 20208685, 20208686, 20208687, 20208688, 20208689, 20208690, 20208691, 20208692, 20208693, 20208695, 20208696, 20208697, 20208698, 20208699, 20208701, 20208703, 20208704, 20219079, 20219080, 20219081, 20219082, 20219083, 20219084, 20219085, 20219086, 20219087, 20219088, 20219089, 20219090, 20219091, 20219092, 20219093,
- Company location
- Plano, TX
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0459-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0459-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.