Home › MEDTRONIC, INC. › Symplicity Spyral™
Symplicity Spyral™
MEDTRONIC, INC. · Model RDN016 · UDI-DI 00763000354466
QYI
Prescription
0
510(k) clearances
41
Adverse events
2
Recalls
7
Facilities
Description
SPYRAL CATHETER RDN016 US COMMERCIAL
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. |
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.