CADDRecalls & reported problems across all models
Icu Medical, Inc. · 123 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
CADD models — page 2
123 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- CADD 21-7057-24Pump, infusion, pca7 reports
- CADD 21-7083-24Set, administration, intravascular7 reports
- CADD 21-2188-25Pump, infusion7 reports
- CADD 21-7062-24Set, administration, intravascular6 reports
- CADD 21-2125-0105-01Pump, infusion6 reports
- CADD 21-7045-24Set, administration, intravascular4 reports
- CADD 21-7060-24Set, administration, intravascular4 reports
- CADD 21-2130-51Pump, infusion, pca4 reports
- CADD 21-2120-0103-00Pump, infusion4 reports
- CADD 21-7095-24Set, administration, intravascular3 reports
- CADD 21-7384-24Set, administration, intravascular3 reports
- CADD 21-7365-24Set, administration, intravascular3 reports
- CADD 80-01-040Warmer, blood, non-electromagnetic radiation3 reports
- CADD 21-7023-24Set, administration, intravascular2 reports
- CADD 21-2120-0102-92Pump, infusion2 reports
- CADD 21-7021-24Set, administration, intravascular1 report
- CADD 21-7100-24Pump, infusion1 report
- CADD 21-7081V-01Set, administration, intravascular1 report
- CADD 21-7107-24Set, administration, intravascular1 report
- CADD 21-2145-01Pump, infusion, pca1 report
- CADD 21-2189-25Pump, infusion1 report
- CADD 21-2165-64Pump, infusion, pca1 report
- CADD 21-7665-24Administrations sets with neuraxial connectors1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page