Home › ICU MEDICAL, INC. › Medex
Medex
ICU MEDICAL, INC. · Model MX447 · UDI-DI 10351688507495
KRK
Prescription
9
510(k) clearances
15
Adverse events
2
Recalls
1
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-02-23 | Carefusion 2200 Inc | The integrity of the sterile packaging is potentially compromised. |
| 2005-11-18 | Medex Inc | The product is labeled as 'Latex Free' , however,one of the components of the finished product may contain latex. |
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.