Home › MEDTRONIC, INC. › IN.PACT™ AV
IN.PACT™ AV
MEDTRONIC, INC. · Model IAV07004013P · UDI-DI 00763000233136
PRC
Prescription
0
510(k) clearances
525
Adverse events (8 deaths)
1
Recalls
8
Facilities
Description
DCB IAV07004013P 07.00 L040 UL1300 US
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-03-23 | Medtronic Vascular, Inc. | Packaging for Balloon Catheters may be damaged resulting in loss of sterility. |
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.