Medtronic Neuromodulation: 54 recalls on record
Recalls filed with 1 agency: FDA (54).
First recall on record: December 19, 2012. Most recent: June 3, 2026.
Risk classification: Class I: 14 · Class II: 39 · Class III: 1
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| April 10, 2013 | FDA | Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is indicated for the t…Z-1031-2013 | Z-1031-2013 |
| December 26, 2012 | FDA | Medtronic, DBS Extension Kit for Deep Brain Stimulation, Catalog # 7482, 37085, 37086. Rx…Z-0567-2013 | Z-0567-2013 |
| December 19, 2012 | FDA | Medtronic SynchroMed II, Model 8637, (The SynchroMed¿ II Pump is supplied in 20 ml or 40 …Z-0497-2013 | Z-0497-2013 |
| December 19, 2012 | FDA | SynchroMed EL, models 8626-10, 8626L-10, 8626-18, 8626L-18, 8627-10, 8627L-10, 8627-18, 8…Z-0496-2013 | Z-0496-2013 |
Questions about this company
- How many recalls does Medtronic Neuromodulation have?
- Recalert has 54 U.S. recalls on record for Medtronic Neuromodulation, published between December 19, 2012 and June 3, 2026.
- Which agencies have handled Medtronic Neuromodulation recalls?
- Medtronic Neuromodulation appears as the recalling firm in recalls from: FDA (54).
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