Home › MEDTRONIC XOMED, INC. › PROPEL
PROPEL
MEDTRONIC XOMED, INC. · Model 50011- · UDI-DI 00763000710392
0
510(k) clearances
48
Adverse events
1
Recalls
4
Facilities
Description
IMPLANT 50011- PROPEL CONTOUR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-10-21 | Intersect ENT, Inc. | Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI. |
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.