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Symplicity G3™
MEDTRONIC, INC. · Model RDNG3A · UDI-DI 00763000387020
QYI
Prescription
0
510(k) clearances
46
Adverse events
2
Recalls
7
Facilities
Description
GENERATOR RDNG3A G3SV5.1 US JP CA
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-01-29 | ReCor Medical Inc. | Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. |
| 2026-01-29 | ReCor Medical Inc. | Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. |
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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.