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MEDTRONIC, INC. · Model 33TH59L · UDI-DI 00763000498795
MRU
Prescription
0
510(k) clearances
2,909
Adverse events (16 deaths)
2
Recalls
9
Facilities
Description
LIT 33TH59L DYSTONIA EMANUALS EN
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-03-30 | Medtronic Neuromodulation | The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system. |
| 2013-02-08 | Medtronic Neuromodulation | There is a potential for lead damage due to the use of the lead cap provided in DBS and Dystonia kits. Medtronic has received reports of DBS leads being damaged at the connector e |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.