Home › MEDTRONIC PS MEDICAL, INC. › Duet®
Duet®
MEDTRONIC PS MEDICAL, INC. · Model 46914 · UDI-DI 00763000428754
1
510(k) clearances
29
Adverse events
5
Recalls
6
Facilities
Description
EDMS DUET 46914 SMARTSITE SITES
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-01-22 | Medtronic Neurosurgery | Potential for catheter disconnection from the patient line stopcock connectors. |
| 2024-01-22 | Medtronic Neurosurgery | Potential for catheter disconnection from the patient line stopcock connectors. |
| 2024-01-22 | Medtronic Neurosurgery | Potential for catheter disconnection from the patient line stopcock connectors. |
| 2024-01-22 | Medtronic Neurosurgery | Potential for catheter disconnection from the patient line stopcock connectors. |
| 2024-01-22 | Medtronic Neurosurgery | Potential for catheter disconnection from the patient line stopcock connectors. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.