Home › MEDTRONIC, INC. › Valve Handle 7420
Valve Handle 7420
MEDTRONIC, INC. · Model 7420 · UDI-DI 00763000582906
10
510(k) clearances
2
Adverse events
1
Recalls
13
Facilities
Description
HANDLE 7420 VLV HNDLE 234MM CEM GLOBAL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2002-04-30 | Carbomedics, Inc | Excessive cleaning and resterilization cause cracking and crazing of device causing the device to malfunction during 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.